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469-14-7

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469-14-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 469-14-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 469-14:
(5*4)+(4*6)+(3*9)+(2*1)+(1*4)=77
77 % 10 = 7
So 469-14-7 is a valid CAS Registry Number.
InChI:InChI=1/C39H63NO10/c1-18-6-9-26-19(2)29-27(40(26)16-18)15-25-23-8-7-21-14-22(10-12-38(21,4)24(23)11-13-39(25,29)5)48-37-34(46)32(44)35(28(17-41)49-37)50-36-33(45)31(43)30(42)20(3)47-36/h7,18-20,22-37,41-46H,6,8-17H2,1-5H3/t18-,19+,20-,22?,23+,24?,25-,26+,27-,28+,29-,30-,31+,32+,33+,34+,35+,36-,37+,38-,39-/m0/s1

469-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name solanidine 3-O-α-L-rhamnopyranosyl-(1->4)-β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names β2-chaconine

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:469-14-7 SDS

469-14-7Relevant articles and documents

Thermal degradation of glycosides. I. Degradation of typical triterpenoid and steroid glycosides

Higuchi,Kitamura,Komori

, p. 638 - 646 (1986)

-

ALKALOIDS OF Rhinopetalum stenantherum. II. THE STRUCTURE OF STENANTHINE AND STENANTHIDINE

Samikov, K.,Rashkes, Ya. V.,Shakirov, R.,Yunusov, S. Yu.

, p. 273 - 278 (2007/10/02)

From a methanolic extract of the epigeal part of Rhinopetalum stenantherum have been isolated β-chaconine (I) and the new glucoalkaloids stenanthine with mp 262-264 deg C, D 46.5 deg, C45H73NO13 (II), and stenanthidine with mp 269-271 deg C, D -47.5 deg, C39H63NO11 (III).On the basis of the facts that partial hydrolysis of trioside (II) formed the biosides (I) and (III), and that on the hydrolysis of the latter the monoside γ-chaconine was found, it may be assumed that stenanthine has the structure of solanidine 3-O-(--D-glucoside), and stenanthidine that of solanidine 3-O-.

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