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L-Leucinamide, N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl-L-phenylalanyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75286-45-2

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75286-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75286-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,8 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75286-45:
(7*7)+(6*5)+(5*2)+(4*8)+(3*6)+(2*4)+(1*5)=152
152 % 10 = 2
So 75286-45-2 is a valid CAS Registry Number.

75286-45-2SDS

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 tert-butyl N-[(2S)-1-[[(2S)-1-[[(2S)-1-amino-4-methyl-1-oxopentan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1-oxopropan-2-yl]carbamate

1.2 Other means of identification

Product number -
Other names L-Leucinamide,N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl-L-phenylalanyl

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:75286-45-2 SDS

75286-45-2Downstream Products

75286-45-2Relevant academic research and scientific papers

Chymotrypsin suspended in organic solvents with salt hydrates is a good catalyst for peptide synthesis from mainly undissolved reactants

Kuhl,Hallinge,Jakubke

, p. 5213 - 5216 (2007/10/02)

Chymotrypsin powder suspended in organic solvents in the presence of Na2CO3.10H2O catalyses peptide synthesis from X-Ala-Phe-OMe and Leu-NH2 (X = Boc or Z). The reaction proceeds best in the most non-polar solve

SYNTHESIS OF CHIRAL OLIGOPEPTIDES BY MEANS OF CATALYTIC ASYMMETRIC HYDROGENATION OF DEHYDROPEPTIDES

Ojima, Iwao,Yoda, Noriko,Yatabe, Momoko,Tanaka, Toshiyuki,Kogure, Tetsuo

, p. 1255 - 1268 (2007/10/02)

Asymmetric hydrogenation of Ac-ΔTyr(Ac)-(S)-Ala-Gly-OMe (6), Ac-ΔTyr(Ac)-(R)-Ala-Gly-(S)-Phe-OMe (7), Ac-ΔPhe-NH-CH(R)-CH2-OCH2Ph (10), HCO-ΔPhe-(S)-Leu-OMe (16), X-AA-ΔPhe-AA'-OMe ( 5: X=tBOC, CBZ, CF3CO; AA, AA'= α-amino acid ), and t

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