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TFMB-(S)-2-HG - ≥99% , CAS No.1445703-64-9

CAS: 1445703-64-9 Cat. No.: T651419 Molecular Weight: 288.22 PubChem CID: 99940754
COA
TFMB-(S)-2-HG - ≥99% CAS No(1445703-64-9) by Aladdin Scientific
AVAILABLE TO ORDER
GRADE & PURITY ≥99%
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
★
 ·  off list, applied to all prices below.
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Status
Price
Qty
5mg
T651419-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$29.90

$44.90
Save $15.00 (33.41%)
10mg
T651419-10mg
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$52.90

$79.90
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25mg
T651419-25mg
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$114.90

$172.90
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50mg
T651419-50mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$195.90

$293.90
Save $98.00 (33.34%)
100mg
T651419-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$331.90

$497.90
Save $166.00 (33.34%)
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SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solution Calculators Reviews
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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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.

Overview

TFMB-(S)-2-HG is a potent inhibitor of the 5'-methylcytosine hydroxylase TET2. TFMB-(S)-2-HG also inhibits the EglN prolyl hydroxylases. TFMB-(S)-2-HG has the potential for the research of acute myeloid leukemia (AML).

Form:Solid

Specifications

Specifications & Purity
≥99%
Biochemical and Physiological Mechanisms
TFMB-(S)-2-HG is a potent inhibitor of the 5'-methylcytosine hydroxylase TET2 . TFMB-(S)-2-HG also inhibits the EglN prolyl hydroxylases. TFMB-(S)-2-HG has the potential for the research of acute myeloid leukemia (AML).
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥99%
Names and Identifiers
Canonical SmilesC1CC(=O)OC1C(=O)OCC2=CC(=CC=C2)C(F)(F)F
IUPAC Name[3-(trifluoromethyl)phenyl]methyl (2S)-5-oxooxolane-2-carboxylate
InChIKeyUXTLNUGKDZMPTC-JTQLQIEISA-N
INCHI1S/C13H11F3O4/c14-13(15,16)9-3-1-2-8(6-9)7-19-12(18)10-4-5-11(17)20-10/h1-3,6,10H,4-5,7H2/t10-/m0/s1
Isomeric SMILES C1CC(=O)O[C@@H]1C(=O)OCC2=CC(=CC=C2)C(F)(F)F
PubChem CID 99940754
Molecular Weight 288.22

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
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzyloxycarbonyls
Intermediate Tree Nodes Not available
Direct ParentBenzyloxycarbonyls
Alternative Parents Trifluoromethylbenzenes  Gamma butyrolactones  Dicarboxylic acids and derivatives  Oxolanes  Carboxylic acid esters  Oxacyclic compounds  Organofluorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Alkyl fluorides  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Benzyloxycarbonyl - Trifluoromethylbenzene - Dicarboxylic acid or derivatives - Gamma butyrolactone - Oxolane - Carboxylic acid ester - Lactone - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Alkyl halide - Hydrocarbon derivative - Organic oxide - Alkyl fluoride - Carbonyl group - Organic oxygen compound - Organohalogen compound - Organofluoride - Organooxygen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzyloxycarbonyls. These are organic compounds containing a carbonyl group substituted with a benzyloxyl group.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SolubilityDMSO : 100 mg/mL (346.96 mM; Need ultrasonic)
Solution Calculators
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