Welcome to LookChem.com Sign In|Join Free
  • or
METHYL 2-AMINO-3-(4-PHENYLPHENYL)PROPANOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

515158-71-1

Post Buying Request

515158-71-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

515158-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 515158-71-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,5,1,5 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 515158-71:
(8*5)+(7*1)+(6*5)+(5*1)+(4*5)+(3*8)+(2*7)+(1*1)=141
141 % 10 = 1
So 515158-71-1 is a valid CAS Registry Number.

515158-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-([1,1'-biphenyl]-4-yl)-2-aminopropanoate

1.2 Other means of identification

Product number -
Other names methyl 2-amino-3-(biphenyl-4-yl)propanoate

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:515158-71-1 SDS

515158-71-1Relevant academic research and scientific papers

METHOD FOR PREPARING D-4,4'-BIPHENYLALANINE ALKYL ESTER OR L-4,4'-BIPHENYLALANINE ALKYL ESTER FROM DL-4,4'-BIPHENYLALANINE ALKYL ESTER

-

Paragraph 0068; 0069; 0070; 0071; 0072; 0073, (2019/05/15)

A method of preparing D-4,4′-biphenylalanine alkyl ester or L-4,4′-biphenylalanine alkyl ester by subjecting DL-4,4′-biphenylalanine alkyl ester to optical resolution using chiral diaroyl tartaric acid as an optical resolving agent is provided.

A biphenyl alanine derivative preparation method

-

Paragraph 0030; 0043; 0046; 0049; 0052; 0055;0058; 0062-0064, (2018/05/24)

The invention relates to a preparation method of a compound represented by the formula (i); and the compound represented by the formula (i) is prepared by taking glycine methyl ester or hydrochloride thereof as the starting material through benzaldehyde protection, benzyl chloride biphenyl alkylation and deprotection. According to the invention, the starting material is easy to obtain and low in cost; furthermore, an intermediate related in the reaction process is unnecessary to separate and purify; the preparation method is simple to operate and moderate in reaction condition; and therefore, the preparation method is applied to industrialized mass production.

BISAMIDE COMPOUNDS AS ALLOSTERIC EFFECTORS FOR REDUCING THE OXYGEN-BINDING AFFINITY OF HEMOGLOBIN

-

, (2016/12/01)

This invention relates to compounds of Formula (I) and pharmaceutically acceptable salts thereof, which are allosteric effectors that reduce the oxygen-binding affinity of hemoglobin, which can enhance the efficacy of radiation therapy for cancer and which are useful for the treatment of ischemia and other conditions.

BISAMIDE COMPOUNDS AS ALLOSTERIC EFFECTORS FOR REDUCING THE OXYGEN-BINDING AFFINITY OF HEMOGLOBIN

-

, (2015/07/23)

This invention relates to compounds of Formula (I) and pharmaceutically acceptable salts thereof, which are allosteric effectors that reduce the oxygen-binding affinity of hemoglobin, which can enhance the efficacy of radiation therapy for cancer and which are useful for the treatment of ischemia and other conditions.

Synthesis of aromatic α-aminoesters: Palladium-catalyzed long-range arylation of primary Csp3-H bonds

Aspin, Sam,Goutierre, Anne-Sophie,Larini, Paolo,Jazzar, Rodolphe,Baudoin, Olivier

, p. 10808 - 10811 (2013/01/15)

Remote control: The title reaction for β-Iζ arylation of α-amino esters with aryl bromides is described. This reaction, which occurs selectively at the terminal position of linear alkyl chains, gives rise to synthetically useful (hetero)arylalanines and homologues after debenzylation (see scheme). Copyright

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 515158-71-1