BTZ043 Racemate - ≥98% , CAS No.957217-65-1

CAS: 957217-65-1 Cat. No.: B412687 Peso molecular: 431.4
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
4-04-00-01412 (Beilstein Handbook Reference) | BTZ043 Racemate | BTZ043,BTZ038, BTZ044 | CCG-269019 | Benzothiazinone 10526038 | SCHEMBL1752396 | DTXSID80678524 | MS-27672 | 2-[2-methyl-1,4-dioxa-8-azaspiro[4.5]dec-8-yl]-8-nitro-6-(trifluoromethyl)-4h-1,3
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5mg
B412687-5mg
2
129,90US$
10mg
B412687-10mg
2
228,90US$
25mg
B412687-25mg
2
457,90US$
50mg
B412687-50mg
2
704,90US$
100mg
B412687-100mg
2
1.127,90US$
200mg
B412687-200mg
2
1.917,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Product Describtion:

BTZ043 racemate is adecaprenylphosphoryl-β-D-ribose 2'-epimerase (DprE1)inhibitor acting as a new antimycobacterial agent that kill Mycobacterium tuberculosis.


 

Specifications

Sinónimos
4-04-00-01412 (Beilstein Handbook Reference) | BTZ043 Racemate | BTZ043, BTZ038, BTZ044 | CCG-269019 | Benzothiazinone 10526038 | SCHEMBL1752396 | DTXSID80678524 | MS-27672 | 2-[2-methyl-1, 4-dioxa-8-azaspiro[4.5]dec-8-yl]-8-nitro-6-(trifluoromethyl)-4h-1, 3
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504770919
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504770919
Sonrisas canónicasCC1COC2(O1)CCN(CC2)C3=NC(=O)C4=C(S3)C(=CC(=C4)C(F)(F)F)[N+](=O)[O-]
IUPAC Name2-(3-methyl-1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-8-nitro-6-(trifluoromethyl)-1,3-benzothiazin-4-one
InChIKeyGTUIRORNXIOHQR-UHFFFAOYSA-N
INCHI1S/C17H16F3N3O5S/c1-9-8-27-16(28-9)2-4-22(5-3-16)15-21-14(24)11-6-10(17(18,19)20)7-12(23(25)26)13(11)29-15/h6-7,9H,2-5,8H2,1H3
Isómeros SMILES CC1COC2(O1)CCN(CC2)C3=NC(=O)C4=C(S3)C(=CC(=C4)C(F)(F)F)[N+](=O)[O-]
Peso molecular 431.4
Reaxy-Rn 13034878
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13034878&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseBenzothiazines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzothiazines
Alternative Parents Azaspirodecane derivatives  Dialkylarylamines  Nitroaromatic compounds  Ketals  Benzenoids  Piperidines  Heteroaromatic compounds  1,3-dioxolanes  Organic oxoazanium compounds  Oxacyclic compounds  Propargyl-type 1,3-dipolar organic compounds  Azacyclic compounds  Organic oxides  Organopnictogen compounds  Hydrocarbon derivatives  Alkyl fluorides  Organic salts  Organofluorides  Organic cations  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Azaspirodecane - Benzothiazine - Nitroaromatic compound - Dialkylarylamine - Ketal - Piperidine - Benzenoid - Meta-dioxolane - Heteroaromatic compound - C-nitro compound - Organic nitro compound - Acetal - Organic oxoazanium - Oxacycle - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organofluoride - Organic nitrogen compound - Organohalogen compound - Organic oxide - Alkyl fluoride - Alkyl halide - Organic oxygen compound - Organic salt - Organopnictogen compound - Organic cation - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzothiazines. These are organic compounds containing a benzene fused to a thiazine ring (a six-membered ring with four carbon atoms, one nitrogen atom and one sulfur atom).
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FECH Tchem Ferrochelatase, mitochondrial (678 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HMBS Tbio Porphobilinogen deaminase (404 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium avium (4587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycolicibacterium smegmatis (8003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vero (26788 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot NumberCertificate TypeFechaArticulo
G2206063Certificate of AnalysisJan 20, 2026 B412687
G2206074Certificate of AnalysisJan 20, 2026 B412687
G2206075Certificate of AnalysisJan 20, 2026 B412687
G2206076Certificate of AnalysisJan 20, 2026 B412687
G2206077Certificate of AnalysisJan 20, 2026 B412687
G2206078Certificate of AnalysisJan 20, 2026 B412687
Propiedades químicas y físicas
Peso molecular431.400 g/mol
XLogP32.900
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count9
Rotatable Bond Count1
Exact Mass431.076 Da
Monoisotopic Mass431.076 Da
Topological Polar Surface Area122.000 Ų
Heavy Atom Count29
Formal Charge0
Complexity720.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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