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13,28-Epoxyoleanane-3β,16α-diol is a naturally occurring triterpenoid compound, characterized by its unique chemical structure featuring an epoxy group at the 13,28 positions and hydroxyl groups at the 3β and 16α positions. 13,28-Epoxyoleanane-3β,16α-diol is typically found in plants and has been the subject of research due to its potential biological activities, such as anti-inflammatory and anticancer properties. The specific arrangement of functional groups in its structure contributes to its pharmacological effects, making it a compound of interest in the field of natural product chemistry and drug discovery.

2611-08-7

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2611-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2611-08-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2611-08:
(6*2)+(5*6)+(4*1)+(3*1)+(2*0)+(1*8)=57
57 % 10 = 7
So 2611-08-7 is a valid CAS Registry Number.

2611-08-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,3aS,5aS,5bS,7aR,9S,11aS,11bS,13aR,13bS)-1-(3-hydroxyprop-1-en-2-yl)-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,9-diol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2611-08-7 SDS

2611-08-7Relevant academic research and scientific papers

Saponins from the Roots of P. elatior (L.) Schreber. - Constitution of a Minor Saponin and Revision of the Sugar Chain of the Main Saponin

Tschesche, Rudolf,Wagner, Rosemarie,Widera, Wolfgang

, p. 993 - 1000 (2007/10/02)

From the roots and rhizomes of Primula elatior the main saponin (PS 4) and four minor saponins were isolated.In the case of one (PS 3) of the minor saponins, the genuine aglycon of which was identified as protoprimulagenin A (1), the structure of the sugar chain consisting of D-glucose, D-glucuronic acid, D-galactose, and L-rhamnose has been established.The structure of the sugar chain of the main saponin has been revised.

SYNTHESES OF AMINOCYCLITOLS AND AMINOCYCLITOL-OLIGOGLYCOSIDES FROM URONIC ACIDS AND GLUCURONIDE-SAPONINS BY MEANS OF AN ELECTROLYTIC DECARBOXYLATION REACTION

Kitagawa, Isao,Kamigauchi, Toshiyuki,Shirakawa, Kiyoharu,Ikeda, Yoshiharu,Ohmori, Hidenobu,Yoshikawa, Masayuki

, p. 349 - 354 (2007/10/02)

By use of the electrolytic decarboxylation reaction as the key step, aminocyclitols (6b, 7b, 8b, 10b, 14b) and aminocyclitol-oligoglycosides (e.g. 18) have been conveniently synthesized from uronic acids (1, 9, 12) and glucuronide-saponins (e.g. 15).The conversions include the first syntheses of optically active D-neo- and L-neo-nitrocyclitols (10, 14).

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