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85889-27-6

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85889-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85889-27-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,8 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85889-27:
(7*8)+(6*5)+(5*8)+(4*8)+(3*9)+(2*2)+(1*7)=196
196 % 10 = 6
So 85889-27-6 is a valid CAS Registry Number.

85889-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-O-β-D-glucuronopyranoside of hederagenin

1.2 Other means of identification

Product number -
Other names 3-O-β-D-glucuronopyranosylhederagenin

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:85889-27-6 SDS

85889-27-6Relevant articles and documents

TRITERPENE GLYCOSIDES OF Climacoptera transoxana. II. THE STRUCTURE OF COPTEROSIDE D

Annaev, Ch.,Isamukhamedova, M.,Abubakirov, N. K.

, p. 425 - 428 (1983)

A new triterpene glycoside, copteroside D, has been isolated from the epigeal part of Climacoptera transoxana (Iljin) Botsch.On the basis of chemical transformations and physicochemical characteristics, copteroside D has been ascribed the structure of hederagenin 28-O-β-D-glucopyranoside 3-O-.

TRITERPENE GLYCOSIDES OF Climacoptera transoxana. III. THE STRUCTURES OF COPTEROSIDES E AND F

Annaev, Ch.,Isaev, M. I.,Abubakirov, N. K.

, p. 560 - 564 (2007/10/02)

New triterpene glycosides have been isolated from the epigeal part of Climacoptera transoxana (Iljin) Botsch. - copterosides E and F.According to chemical transformations and physicochemical characteristics, copteroside E has the structure of oleanolic acid 28-O-β-D-glucopyranoside 3-O-2)>-4)>-β-D-glucuronopyranoside> and copteroside F that of hederagenin 28-O-β-D-glucopyranoside 3-O-2)>-4)>-β-D-glucopyranoside>.

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