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103000-77-7

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103000-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103000-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,0 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103000-77:
(8*1)+(7*0)+(6*3)+(5*0)+(4*0)+(3*0)+(2*7)+(1*7)=47
47 % 10 = 7
So 103000-77-7 is a valid CAS Registry Number.
InChI:InChI=1/C42H62O16/c1-37(2)21-8-11-42(7)31(20(43)16-18-19-17-39(4,36(53)54)13-12-38(19,3)14-15-41(18,42)6)40(21,5)10-9-22(37)55-35-30(26(47)25(46)29(57-35)33(51)52)58-34-27(48)23(44)24(45)28(56-34)32(49)50/h16,19,21-31,34-35,44-48H,8-15,17H2,1-7H3,(H,49,50)(H,51,52)(H,53,54)/t19-,21-,22-,23-,24-,25-,26-,27+,28-,29-,30+,31+,34-,35+,38+,39-,40-,41+,42+/m0/s1

103000-77-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3β)-30-Hydroxy-11,30-dioxoolean-12-en-3-yl 2-O-β-D-glucopyranuro nosyl-β-D-glucopyranosiduronic acid

1.2 Other means of identification

Product number -
Other names DerMacrin

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:103000-77-7 SDS

103000-77-7Downstream Products

103000-77-7Relevant academic research and scientific papers

METHOD FOR PRODUCING GLYCYRRHIZINIC ACID AND GALACTURO GLYCYRRHIZINIC ACID, AND INTERMEDIATE USED FOR THE PRODUCTION METHOD

-

Paragraph 0039; 0045, (2018/07/28)

PROBLEM TO BE SOLVED: To provide a synthesis method that makes it possible to produce high-purity glycyrrhizinic acid or galacturo glycyrrhizinic acid, simply and in high yields. SOLUTION: A production method includes performing glycosylation of position-3 hydroxy group of glycyrrhetinic acid, then performing selective galactosylation or glycosylation at position-2', and through deprotection, performing selective oxidation of a primary hydroxy group. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

TRANSFORMATIONS OF GLYCYRRHIZIC ACID. III.* SYNTHESIS OF NEW GLYCOPEPTIDES CONTAINING METHYL ESTERS OF AMINO ACIDS

Baltina, L. A.,Tolstikov, G. A.

, p. 1115 - 1120 (2007/10/02)

A new selective method has been proposed for the preparation of glycopeptides of β-glycyrrhizic acid (I) containing fragments of methyl esters of amino acids by reacting tris-N-hydroxysuccinimidic ester of a glycoside, obtained in situ using N,N'-dicyclohexylcarbodiimide, with hydrochlorides of methyl esters of amino acids or dipeptides in the presence of triethylamine.

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