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98474-78-3

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98474-78-3 Usage

Uses

Pseudoginsenoside RT5 is a novel active ginsenoside from Ginseng with protective effect against cisplatin (CDDP)?-?induced nephrotoxicity in vivo. Pseudoginsenoside RT is a metabolite of pseudo-?ginsenoside F11.

Check Digit Verification of cas no

The CAS Registry Mumber 98474-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,4,7 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98474-78:
(7*9)+(6*8)+(5*4)+(4*7)+(3*4)+(2*7)+(1*8)=193
193 % 10 = 3
So 98474-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C36H62O10/c1-31(2)23(39)10-12-33(5)22-15-19(38)25-18(36(8)14-11-24(46-36)32(3,4)43)9-13-34(25,6)35(22,7)16-20(29(31)33)44-30-28(42)27(41)26(40)21(17-37)45-30/h18-30,37-43H,9-17H2,1-8H3/t18-,19+,20-,21+,22+,23-,24+,25-,26+,27-,28+,29-,30+,33+,34+,35+,36-/m0/s1

98474-78-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Pseudoginsenoside RT5

1.2 Other means of identification

Product number -
Other names pseudo-ginsenosides-RT4

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:98474-78-3 SDS

98474-78-3Upstream product

98474-78-3Downstream Products

98474-78-3Relevant articles and documents

Synthesis of Ocotillol-Type Ginsenosides

Shen, Renzeng,Cao, Xin,Laval, Stephane,Sun, Jiansong,Yu, Biao

, p. 10279 - 10294 (2016/11/17)

A total of 14 ocotillol-type ginsenosides were conveniently synthesized employing glycosylation of ocotillol sapogenin derivatives with glucosyl ortho-alkynylbenzoate donors under the promotion of a gold(I) catalyst as the key step. Relying on a rational protecting group strategy and the unexpected regioselectivity of the glycosylation of the 3,25-diol sapogenins (2a/2b, 5a/5b) for the tertiary 25-OH, mono 3-O-glucosyl ocotillol-PPD, 6-O-glucosyl ocotillol-PPT, 25-O-glucosyl ocotillol-PPD/PPT and 3,25-di-O-glucosyl ocotillol-PPD/PPT ginsenosides were prepared in which the configuration at the C-24 is either R or S.

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