Fumagillol - ≥98% , CAS No.108102-51-8

Name: Fumagillol - ≥98% , CAS No.108102-51-8
SKU: F356712
Availability: InStock

CAS: 108102-51-8 Cat. No.: F356712 Formula: C₁₆H₂₆O₄ Peso molecolare: 282.38

COA

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Fumagillol - ≥98% CAS No(108102-51-8) by Aladdin Scientific

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Disponibile su ordine

GRADE & PURITY ≥98%

Synonyms

(3R,4S,5S,6R)-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-enyl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-ol | (-)-Fumagillol | SCHEMBL2553407 | 1-OXASPIRO(2.5)OCTAN-6-OL, 5-METHOXY-4-((2R,3R)-2-METHYL-3-(3-METHYL-2-BUTEN-1-YL)-2-OXIRANYL)-, (3R,4S,5S,6R)- |

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica Specifications Nomi e identificatori Documentazione Advanced Data Taxonomic Classification Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Calcolatori di soluzioni Recensioni

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Why this grade

≥98% 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.

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Quality documents

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

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Literature proof

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

Panoramica

Fumagillol is a direct precursor of the potent angiogenesis inhibitors TNP-470 and fumagillin

Specifications

Sinonimi

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥98%

Nomi e identificatori

Pubchem Sid

504757918

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504757918

Sorrisi canonici

CC(=CCC1C(O1)(C)C2C(C(CCC23CO3)O)OC)C

IUPAC Name

(3R,4S,5S,6R)-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-enyl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-ol

InChIKey

CEVCTNCUIVEQOY-JQOWZUPLSA-N

INCHI

1S/C16H26O4/c1-10(2)5-6-12-15(3,20-12)14-13(18-4)11(17)7-8-16(14)9-19-16/h5,11-14,17H,6-9H2,1-4H3/t11-,12-,13-,14-,15+,16+/m1/s1

Isomeri SMILES

CC(=CC[C@@H]1[C@@](O1)(C)[C@H]2[C@@H]([C@@H](CC[C@]23CO3)O)OC)C

Peso molecolare

282.38

Reaxy-Rn

216601

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=216601&ln=

Documentazione

📋 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

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Classe Organooxygen compounds
    - Subclass Alcohols and polyols

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Classe	Organooxygen compounds
Subclass	Alcohols and polyols
Intermediate Tree Nodes	Not available
Direct Parent	Cyclic alcohols and derivatives
Alternative Parents	Secondary alcohols Oxacyclic compounds Epoxides Dialkyl ethers Hydrocarbon derivatives
Molecular Framework	Aliphatic heteropolycyclic compounds
Substituents	Cyclic alcohol - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Ether - Oxirane - Dialkyl ether - Hydrocarbon derivative - Aliphatic heteropolycyclic compound
Descrizione	This compound belongs to the class of organic compounds known as cyclic alcohols and derivatives. These are organic compounds containing an aliphatic ring substituted with at least one hydroxyl group.
External Descriptors	sesquiterpenoid
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Struttura 3D

Obiettivi associati (umani)

A498 (42825 Activities)

Lot Number	Certificate Type	Data	Oggetto
L2525007	Certificate of Analysis	Jan 06, 2026	F356712
K2211432	Certificate of Analysis	Aug 11, 2022	F356712
K2211440	Certificate of Analysis	Aug 11, 2022	F356712
K2211452	Certificate of Analysis	Aug 11, 2022	F356712
K2211457	Certificate of Analysis	Aug 11, 2022	F356712
K2211466	Certificate of Analysis	Aug 11, 2022	F356712
K2211472	Certificate of Analysis	Aug 11, 2022	F356712

Indice di rifrazione	n20D1.53 (Predicted)
Punto di ebollizione (°C)	~390.0° C at 760 mmHg (Predicted)
Punto di fusione (°C)	119.35° C (Predicted)
Peso molecolare	282.370 g/mol
XLogP3	1.700
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	4
Exact Mass	282.183 Da
Monoisotopic Mass	282.183 Da
Topological Polar Surface Area	54.500 Å²
Heavy Atom Count	20
Formal Charge	0
Complexity	417.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	6
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1