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1,4-Dioxa-8,11-diazacyclohexadec-13-ene-2,5,9,12-tetrone, 10-[(3-chloro-4-methoxyphenyl)methyl]-16-[(1R,2E)-1-methyl-3-phenyl-2 -propenyl]-3-(2-methylpropyl)-7-(phenylmethyl)-, (3S,7R,10R,13E,16S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193070-88-1

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193070-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193070-88-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,0,7 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 193070-88:
(8*1)+(7*9)+(6*3)+(5*0)+(4*7)+(3*0)+(2*8)+(1*8)=141
141 % 10 = 1
So 193070-88-1 is a valid CAS Registry Number.

193070-88-1SDS

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 (E)-(3S,7R,10R,16S)-7-Benzyl-10-(3-chloro-4-methoxy-benzyl)-3-isobutyl-16-((E)-(R)-1-methyl-3-phenyl-allyl)-1,4-dioxa-8,11-diaza-cyclohexadec-13-ene-2,5,9,12-tetraone

1.2 Other means of identification

Product number -
Other names -

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:193070-88-1 SDS

193070-88-1Downstream Products

193070-88-1Relevant academic research and scientific papers

Synthesis and Biological Evaluation of Novel Cryptophycin Analogs with Modification in the β-Alanine Region

Shih, Chuan,Gossett, Lynn S.,Gruber, Joseph M.,Grossman, C. Sue,Andis, Sherri L.,et al.

, p. 69 - 74 (2007/10/03)

Structure modification of the β-alanine region (fragment C) of the potent antimitotic agent cryptophycin was investigated. This includes: (1) introduction of substituents at the previously unsubstituted C7 position of the macrolide ring and (2) replacement of the (2R)-3-amino-2-methyl-propanoic acid (β-alanine) with various (l)-amino acids to give the corresponding 15-membered unnatural cryptophycin analogs.

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