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tert-butyl 2-(2-amino-3-phenylpropanoyl)hydrazinecarboxylate (non-preferred name) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36261-38-8

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36261-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36261-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,6 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36261-38:
(7*3)+(6*6)+(5*2)+(4*6)+(3*1)+(2*3)+(1*8)=108
108 % 10 = 8
So 36261-38-8 is a valid CAS Registry Number.

36261-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[(2-amino-3-phenylpropanoyl)amino]carbamate

1.2 Other means of identification

Product number -
Other names Hydrazinecarboxylicacid,2-(2-amino-1-oxo-3-phenylpropyl)-,1,1-dimethylethyl ester,(S)-(9CI)

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:36261-38-8 SDS

36261-38-8Downstream Products

36261-38-8Relevant academic research and scientific papers

SOLUTION SYNTHESIS OF THE HEPTADECAPEPTIDE SEQUENCE OF VESPULAKININ 1

Biondi, Laura,Cavaggion, Franco,Filira, Fernando,Rocchi, Raniero

, p. 427 - 434 (2007/10/02)

Solution synthesis is described of the carbohydrate-free heptadecapeptide sequence of vespulakinin 1.The segment condensation strategy has been utilized to assemble the complete sequence.Carboxyl activation has been achieved by the 1-succinimidyl esters m

Synthesis of PHI (Peptide Histidine Isoleucine) and Related Peptides and Immunochemical Confirmation of Amino Acid Residue in Position 24 of PHI with use of the Synthetic Peptides

Nokihara, K.,Yanaihara, C.,Iguchi, K.,Fukata, S.,Tanaka, M.,et al.

, p. 7909 - 7916 (2007/10/02)

An immunochemical approach, using synthetic peptides, was employed to establish the nature of residue 24 in the amino acid sequence of PHI (peptide histidine isoleucine).PHI(20-27) and 24>-PHI(20-27) were synthesized by conventional solutio

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