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128135-31-9

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128135-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128135-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,1,3 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 128135-31:
(8*1)+(7*2)+(6*8)+(5*1)+(4*3)+(3*5)+(2*3)+(1*1)=109
109 % 10 = 9
So 128135-31-9 is a valid CAS Registry Number.

128135-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 4-[(tert-butoxycarbonyl)amino]-5-oxo-6-diazohexanoate

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:128135-31-9 SDS

128135-31-9Relevant articles and documents

CASPASE INHIBITORS AND METHODS OF USE THEREOF

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Paragraph 00264-00266; 00286-00288, (2020/09/19)

Provided herein are compounds of formula (I), compositions comprising the compounds and method of treating various diseases with the compounds and compositions.

FOLDAMER HELIX BUNDLE-BASED MOLECULAR ENCAPSULATION

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Paragraph 00316; 00317, (2017/03/21)

The present description provides compositions and methods for producing therapeutic oligomeric compounds. In another aspect the description provides methods for administering the oligomeric compounds for the treatment and prevention of disease in a mammal

Synthesis of N-urethane protected α-aminoalkyl-α-cyanomethyl ketones; Application to the synthesis of 3-substituted 5-amino-1H-pyrazole tethered peptidomimetics

Sharnabai,Nagendra,Sureshbabu, Vommina V.

scheme or table, p. 1913 - 1918 (2012/09/25)

The preparation of N-protected amino/peptide α-cyanomethyl ketones through cyanation of the corresponding α-bromomethyl ketones is described. The utility of the resulting α-cyanomethyl ketones in the synthesis of 3-substituted-5-amino-1H-pyrazoles has also been demonstrated. In both steps a wide range of N-protected amino/peptide acids has been employed and the products are obtained in good yield. The enantiomeric purity of both the α-cyanomethyl ketones and pyrazoles were confirmed by chiral HPLC analysis of the corresponding Z-protected d- and l-Ala-OH as model substrates. The synthesis of peptide pyrazolecarboxamides is also delineated. Georg Thieme Verlag Stuttgart · New York.

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