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74874-08-1

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  • Ethyl (2R,4R)-1-(nitroglycerine-nitro-L-arginyl)-4-methyl-piperidinecarboxylate hydrochloride

    Cas No: 74874-08-1

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74874-08-1 Usage

Chemical Properties

Off White Solid

Uses

Argatroban intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 74874-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,7 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74874-08:
(7*7)+(6*4)+(5*8)+(4*7)+(3*4)+(2*0)+(1*8)=161
161 % 10 = 1
So 74874-08-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H28N6O5.ClH/c1-3-26-14(23)12-9-10(2)6-8-20(12)13(22)11(16)5-4-7-18-15(17)19-21(24)25;/h10-12H,3-9,16H2,1-2H3,(H3,17,18,19);1H/t10-,11?,12-;/m1./s1

74874-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl (2R,4R)-1-(Nitroglycerine-nitro-L-arginyl)-4-methyl-piperidinecarboxylate hydrochloride

1.2 Other means of identification

Product number -
Other names Argatroban Intermediate

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:74874-08-1 SDS

74874-08-1Downstream Products

74874-08-1Relevant articles and documents

Thrombin inhibitors. 3. Carboxyl-containing amide derivatives of N alpha-substituted L-arginine.

Kikumoto,Tamao,Ohkubo,Tezuka,Tonomura,Okamoto,Hijikata

, p. 1293 - 1299 (2007/10/02)

A series of N alpha-(arylsulfonyl)-L-arginine amide derivatives having carboxamide N-substituents with a carboxyl group was prepared and tested as inhibitors of the clotting activity of thrombin. The most inhibitory compounds were obtained when a carboxyl group was introduced into the carbon next to the amide nitrogen of N alpha-(arylsulfonyl)-L-arginine amide derivatives, e.g., N alpha-(arylsulfonyl)-L-arginyl-N-butyl-, N-(methoxyethyl)- or N-(tetrahydrofurfuryl)glycine and 4-alkyl-1-[N alpha-(arylsulfonyl)-L-arginyl]-2-piperidinecarboxylic acid, with an I50 of 1-3 X 10(-7) M.

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