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N-(2-amino-1-(aminocarbonyl)-3-methylbutyl)histidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134359-69-6

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134359-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134359-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,3,5 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134359-69:
(8*1)+(7*3)+(6*4)+(5*3)+(4*5)+(3*9)+(2*6)+(1*9)=136
136 % 10 = 6
So 134359-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H21N5O3/c1-6(2)9(13)10(11(14)18)17-8(12(19)20)3-7-4-15-5-16-7/h4-6,8-10,17H,3,13H2,1-2H3,(H2,14,18)(H,15,16)(H,19,20)/t8-,9-,10-/m0/s1

134359-69-6SDS

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 (1S,2S)-N-<2-amino-1-(aminocarbonyl)-3-methylbutyl>-L-histidine

1.2 Other means of identification

Product number -
Other names (S)-2-((1S,2S)-2-Amino-1-carbamoyl-3-methyl-butylamino)-3-(1H-imidazol-4-yl)-propionic acid

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:134359-69-6 SDS

134359-69-6Relevant academic research and scientific papers

Synthesis and Biological Activity of Angiotensin II Analogues Containing a Val-His Replacement, ValΨHis

Mohan, Raju,Chou, Yuo-Ling,Bihovsky, Ron,Lumma, William C.,Erhardt, Paul W.,Shaw, Kenneth J.

, p. 2402 - 2410 (2007/10/02)

The dipeptide mimic ValΨHis (4) was incorporated into angiotensin II (AII) analogues to provide an octapeptide saralisn derivative (29) as well as tetrapeptide analogue 19.Three C-terminal tetrapeptides (21, 25, and 28) were also prepared.All

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