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155660-91-6

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155660-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155660-91-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,6,6 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155660-91:
(8*1)+(7*5)+(6*5)+(5*6)+(4*6)+(3*0)+(2*9)+(1*1)=146
146 % 10 = 6
So 155660-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C40H70N2O8/c1-8-11-32(44)23-34-21-27(3)22-35(48-34)24-38(46)42-25-36(45)30(6)39(47)41-19-10-13-37-28(4)16-18-40(50-37)17-9-12-33(49-40)15-14-26(2)20-29(5)31(7)43/h8,11,20,26-28,30-37,43-45H,9-10,12-19,21-25H2,1-7H3,(H,41,47)(H,42,46)/b11-8+,29-20+

155660-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-N-[3-[8-[(E)-6-hydroxy-3,5-dimethylhept-4-enyl]-3-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]propyl]-4-[[2-[6-[(E)-2-hydroxypent-3-enyl]-4-methyloxan-2-yl]acetyl]amino]-2-methylbutanamide

1.2 Other means of identification

Product number -
Other names 3-hydroxy-N-[3-[4-[(E)-6-hydroxy-3,5-dimethylhept-4-enyl]-9-methyl-5,11-dioxaspiro[5.5]undecan-10-yl]propyl]-4-[[2-[6-[(E)-2-hydroxypent-3-enyl]-4-methyloxan-2-yl]acetyl]amino]-2-methylbutanamide

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:155660-91-6 SDS

155660-91-6Downstream Products

155660-91-6Relevant articles and documents

Synthesis of derivatives of potent antitumor bistramides D and A leading to the first crystal structure of natural bistramide D

Bauder, Claude,Biard, Jean-Franois,Solladie, Guy

, p. 1860 - 1862 (2006)

The synthesis of derivatives of potent antitumor bistramides D and A, which led to the first crystal structure of natural bistramide D, was discussed. The absolute configuration of a chemical derivative of bistramide D by radiocrystallographic analysis starting from the natural material was analyzed. The structural assignment of bistramide D was resolved using an alternative strategic scheme, based on studies of derivatives of natural bistramide. The research was focused on the derivatives of the natural bistramide because of the structural complexity of bistramide D and its great number of possible stereoisomer.

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