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N-Benzyloxycarbonyl D-Valine Methyl Ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154674-67-6

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154674-67-6 Usage

Uses

Different sources of media describe the Uses of 154674-67-6 differently. You can refer to the following data:
1. Protected Amino Acid.
2. N-Benzyloxycarbonyl D-Valine Methyl Ester is a protected amino acid.

Check Digit Verification of cas no

The CAS Registry Mumber 154674-67-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,6,7 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 154674-67:
(8*1)+(7*5)+(6*4)+(5*6)+(4*7)+(3*4)+(2*6)+(1*7)=156
156 % 10 = 6
So 154674-67-6 is a valid CAS Registry Number.

154674-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Benzyloxycarbonyl D-Valine Methyl Ester

1.2 Other means of identification

Product number -
Other names methyl (2R)-3-methyl-2-(phenylmethoxycarbonylamino)butanoate

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:154674-67-6 SDS

154674-67-6Downstream Products

154674-67-6Relevant academic research and scientific papers

A mild and efficient chemoselective: N-benzyloxycarbonylation of amines using TBAB a catalyst under solvent-free conditions

Babu, Kothamasu Suresh,Rao, Vidadala Rama Subba,Rao, Ravu Ranga,Babu, Sakhamuri Sivaram,Rao, Janaswami Madhusudana

experimental part, p. 393 - 396 (2009/10/17)

We describe a mild and efficient method for the chemoselective N-benzyloxycarbonylation of amines by treatment amines and aminoesters with benzyloxycarbonyl chloride (Cbz-Cl) in the presence of TBAB under solvent-free in excellent yields. The method is ge

A solid-phase approach to analogues of the antibiotic mureidomycin

Bozzoli, Andrea,Kazmierski, Wieslaw,Kennedy, Gordon,Pasquarello, Alessandra,Pecunioso, Angelo

, p. 2759 - 2763 (2007/10/03)

A library of 80 analogues of the antibacterial compound mureidomycin was prepared using solid-phase chemistry techniques. (C) 2000 Elsevier Science Ltd.

Asymmetric α-Aminoacid Synthesis using Rearrangement of Allylic Trifluoroacetimidates: Synthesis of Thymine Polyoxin C

Chen, Anqi,,Savage, Ian,Thomas, Eric J.,Wilson, Peter D.

, p. 6769 - 6772 (2007/10/02)

Improved procedures are reported for the synthesis of chiral trifluoroacetimidates and are applied to complete a total synthesis of thymine polyoxin C.

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