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87421-27-0

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87421-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87421-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,2 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87421-27:
(7*8)+(6*7)+(5*4)+(4*2)+(3*1)+(2*2)+(1*7)=140
140 % 10 = 0
So 87421-27-0 is a valid CAS Registry Number.

87421-27-0SDS

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 2-<(N-tert-butoxycarbonyl)amino>-3-benzyloxycarbonylbutanamide

1.2 Other means of identification

Product number -
Other names 3-tert-Butoxycarbonylamino-succinamic acid benzyl ester

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:87421-27-0 SDS

87421-27-0Relevant articles and documents

Dehydromicrosclerodermin B and Microsclerodermin J: Total Synthesis and Structural Revision

Melikhova, Ekaterina Y.,Pullin, Robert D. C.,Winter, Christian,Donohoe, Timothy J.

supporting information, p. 9753 - 9757 (2016/08/10)

The total synthesis of dehydromicrosclerodermin B and microsclerodermin J is described. Efficient approaches to the unusual amino acids in the target molecules were developed on the basis of a Negishi coupling (for Trp-2-CO2H) and Blaise reaction (for Pyrr). An incorrect assignment of the pyrrolidinone stereochemistry of both compounds was confirmed by synthesizing epimers of the proposed structures. The spectroscopic data of these epimers were in complete agreement with those for the naturally derived material.

USE OF CSE INHIBITORS FOR THE TREATMENT OF CUTANEOUS INJURIES OR CONDITIONS AND SLEEP-RELATED BREATHING DISORDERS

-

Paragraph 00431, (2014/02/16)

no abstract published

CATHEPSIN CYSTEINE PROTEASE INHIBITORS FOR THE TREATMENT OF VARIOUS DISEASES

-

Page/Page column 38-39, (2011/01/12)

The present invention relates to compounds capable of inhibiting and/or decreasing the activity of one or more cathepsins, thereby treating and/or preventing various disease states associated with one or more cysteine proteases including, but not limited

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