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p-(phenylazo)benzyl chloroformate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55592-99-9

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55592-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55592-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,9 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55592-99:
(7*5)+(6*5)+(5*5)+(4*9)+(3*2)+(2*9)+(1*9)=159
159 % 10 = 9
So 55592-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H11ClN2O2/c15-14(18)19-10-11-6-8-13(9-7-11)17-16-12-4-2-1-3-5-12/h1-9H,10H2/b17-16+

55592-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-phenyldiazenylphenyl)methyl carbonochloridate

1.2 Other means of identification

Product number -
Other names EINECS 259-719-5

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:55592-99-9 SDS

55592-99-9Relevant academic research and scientific papers

α-Ketoester-based photobiological switches: Synthesis, peptide chain extension and assay against α-chymotrypsin

Harvey, Andrew J.,Abell, Andrew D.

, p. 2441 - 2444 (2007/10/03)

The design, synthesis, photoisomerism and biological testing of two peptide-based photoswitchable inhibitors of α-chymotrypsin are presented. The use of a dipeptide recognition sequence gave a 'slow-tight binding' inhibitor, while the introduction of a carbamate linker to the azobenzene gave a modest enhancement in photoswitching of enzyme activity for the photostationary state enriched in the (Z)-isomer over the (E)-isomer.

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