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55533-25-0

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55533-25-0 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 55533-25-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,3 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55533-25:
(7*5)+(6*5)+(5*5)+(4*3)+(3*3)+(2*2)+(1*5)=120
120 % 10 = 0
So 55533-25-0 is a valid CAS Registry Number.

55533-25-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-p(NH-Z)-L-Phe-OH

1.2 Other means of identification

Product number -
Other names Boc-4-(NHCbz)Phe-OH

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:55533-25-0 SDS

55533-25-0Relevant articles and documents

BISAMINO BENZYLPIPERAZINE DIONE, AMIDE ACID POLYMER AND POLYIMIDE, AND HOLLOW POLYIMIDE PARTICLE AND MANUFACTURING METHOD THEREFOR

-

Paragraph 0122; 0123; 0124; 0125, (2019/10/02)

PROBLEM TO BE SOLVED: To provide polyimide which is rigid, easily powdered, and excellent in chemical resistance, heat resistance, or the like, an amide acid polymer useful as a manufacturing intermediate of the polyimide, an amide acid polymer useful as

Development of active center-directed plasmin and plasma kallikrein inhibitors and studies on the structure-inhibitory activity relationship

Teno,Wanaka,Okada,Taguchi,Okamoto,Hijikata-Okunomiya,Okamoto

, p. 1079 - 1090 (2007/10/02)

The molecule of trans-4-aminomethylcyclohexanecarbonylphenylalanine 4- carboxymethylanilide (8), which is a potent and selective inhibitor of plasma kallikrein, can be divided into three parts (P1, P1 and P2), each of which contains one of the rings. In order to study the role of each part in the manifestation of potent and selective inhibitory activity and the relationship between the structure and inhibitory activities toward plasmin, plasma kallikrein, urokinase and thrombin, each part was substituted with various other moieties to give many kinds of analogs and their inhibitory activities against the above enzymes were examined. Among them, trans-4- aminomethylcyclohexanecarbonyl-O-2-bromobenzyloxycarbonyltyrosine 4- acetylanilide (12) inhibited plasmin and plasma kallikrein with IC50 values of 2.3 x 10-7 M and 3.7 x 10-7 M, and K(i) values of 1.2 x 10-7 M and 1.3 x 10-7 M, respectively.

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