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METHYL-(2Z)3-IODO-2N-ACETYL CROTANOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

686744-70-7

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686744-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 686744-70-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,6,7,4 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 686744-70:
(8*6)+(7*8)+(6*6)+(5*7)+(4*4)+(3*4)+(2*7)+(1*0)=217
217 % 10 = 7
So 686744-70-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H10INO3/c1-4(8)6(7(11)12-3)9-5(2)10/h1-3H3,(H,9,10)/b6-4-

686744-70-7SDS

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 METHYL-(2Z)3-IODO-2N-ACETYL CROTANOATE

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:686744-70-7 SDS

686744-70-7Relevant academic research and scientific papers

PEPTIDOMIMETIC SOMATOSTATIN RECEPTOR SUBTYPE 2 LIGANDS AND PET IMAGING AGENTS

-

Page/Page column 22-23, (2010/11/25)

The present invention is directed to compounds useful as peptidomimetics for binding and/or imaging somatostatin subtype 2 receptors, and compositions comprising the compounds. The present invention is also directed to methods of preparing radiolabeled pe

A Versatile Chemo-Enzymatic Route to Enantiomerically Pure β-Branched α-Amino Acids

Roff, Geoffrey J.,Lloyd, Richard C.,Turner, Nicholas J.

, p. 4098 - 4099 (2007/10/03)

A series of diastereoisomers of β-methyl-β-phenylalanine analogues 1a?f have been prepared in enantiomerically pure form using a combination of chemo- and biocatalysis. Starting from l-threonine methyl ester 2, a range of β,β-disubstituted didehydroamino

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