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L-Met-L-Leu-Gly-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14486-11-4

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14486-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14486-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,8 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14486-11:
(7*1)+(6*4)+(5*4)+(4*8)+(3*6)+(2*1)+(1*1)=104
104 % 10 = 4
So 14486-11-4 is a valid CAS Registry Number.

14486-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[(2S)-2-[[(2S)-2-amino-4-methylsulfanylbutanoyl]amino]-4-methylpentanoyl]amino]acetic acid

1.2 Other means of identification

Product number -
Other names H-Met-Leu-Gly-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:14486-11-4 SDS

14486-11-4Downstream Products

14486-11-4Relevant academic research and scientific papers

N-acyl and desamino human calcitonin and analogs thereof

-

, (2008/06/13)

The new hypocalcaemically active peptides of formula I and corresponding compounds in which one or more of the asparagine and glutamic acid radicals are replaced by the aspartic acid or glutamic acid radical and/or the aspartic acid radical is replaced by the asparagine radical, their dimers, especially those in which 2 identical peptide sequences (1-32 and 1'-32') are joined in an anti-parallel arrangement via the cysteine radicals 1,7' and 7,1' by means of a disulfide bond, and derivatives are useful as hypocalcaemic agents and are prepared by splitting off groups protecting at least one amino or one carboxyl group or oxidizing the corresponding sulfides to the disulfides or condensing together adequate peptides.

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