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57539-70-5

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57539-70-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57539-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,3 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57539-70:
(7*5)+(6*7)+(5*5)+(4*3)+(3*9)+(2*7)+(1*0)=155
155 % 10 = 5
So 57539-70-5 is a valid CAS Registry Number.

57539-70-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β,23-dihydroxyolean-12-en-28-oic acid O-α-L-rhamnopyranosyl-(1->4)-O-β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl ester

1.2 Other means of identification

Product number -
Other names cussonoside A

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:57539-70-5 SDS

57539-70-5Downstream Products

57539-70-5Relevant articles and documents

Triterpenoid saponins of Acanthopanax nipponicus leaves

Miyakoshi, Masazumi,Shirasuna, Katsuya,Hirai, Yasuaki,Shingu, Kazushi,Isoda, Susumu,Shoji, Junzo,Ida, Yoshiteru,Shimizu, Torao

, p. 445 - 448 (2007/10/03)

Five new triterpenoid saponins, nipponosides A-E (1, 3-6), were isolated from Acanthopanax nipponicus leaves, along with a known saponin, kalopanaxsaponin G (2). Nipponosides A-E were characterized as the 28-O-α- L-rhamnopyranosyl(1-4)-β-D-glucopyranosyl(16)-β-D-glucopyranosyl ester of 3-oxohederagenin, oleanolic acid 3-O-β-D-glucopyranoside, gypsogenin 3-O- β-D-glucopyranoside, 3β,23,29-trihydroxyolean-12-en-28-oic acid, and 3β,20α,23-trihydroxy-30-nor-olean-12-en-28-oic acid, respectively. The structures of these new compounds were based on chemical and spectral methods.

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