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70156-40-0

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70156-40-0 Usage

General Description

Methyl 3-[(4-Hydroxyphenyl)aMino]propanoate is a chemical compound commonly used in the synthesis of pharmaceutical drugs, particularly those aimed at treating neurological disorders and cardiovascular diseases. It is a derivative of 4-hydroxyphenylalanine, an important amino acid in the human body. Methyl 3-[(4-Hydroxyphenyl)aMino]propanoate plays a crucial role in the functional group of many biologically active molecules and can act as both an electron donor and acceptor. Additionally, it is also used in the production of many agricultural chemicals, such as pesticides and fertilizers. It is important to handle this chemical with care as it can be harmful if ingested, inhaled, or comes into contact with the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 70156-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,5 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70156-40:
(7*7)+(6*0)+(5*1)+(4*5)+(3*6)+(2*4)+(1*0)=100
100 % 10 = 0
So 70156-40-0 is a valid CAS Registry Number.

70156-40-0SDS

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 N-(4-hydroxyphenyl)-β-alanine methyl ester

1.2 Other means of identification

Product number -
Other names Methyl 3-[(4-Hydroxyphenyl)amino]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:70156-40-0 SDS

70156-40-0Relevant articles and documents

Bio-heterogeneous Cu(0)NC@PHA for n-aryl/alkylation at room temperature

Jian Fui, Choong,Lutfor Rahman, Md,Musta, Baba,Sani Sarjadi, Mohd,Sarkar, Shaheen M.,Xin Ting, Tang

, (2021/06/28)

A pure cellulose was derived from waste fibre and it was chemically modified to a hydroxamic acid ligand. The poly(hydroxamic acid) was treated with an aqueous copper solution to afford the greenish stable five-membered copper complex; namely Cu(II)@PHA. Further, the Cu(II)@PHA was treated with a reducing agent hydrazine hydride to give brown colour cellulose supported copper nanocomplex (Cu(0)NC@PHA). The Cu(0)NC@PHA was characterised by ATR-FTIR, FE-SEM & EDS, TEM, ICP-OES, TGA, XRD and XPS analyses. The cellulose-based Cu(0)NC@PHA was used for the n-aryl/alkylation (Michael addition) reaction with a variety of α,β-unsaturated Michael acceptors to produce the corresponding n-aryl/alkyl products with an excellent yield at room temperature. The Cu(0)NC@PHA showed extraordinary stability and it was easily filtered out from the reaction mixture and may potentially recycled up to five times without loss of its original catalytic ability.

SYNTHESIS AND TRANSFORMATIONS OF 1-(4-HYDROXYPHENYL)DIHYDROURACILS

Baltrushis, R. S.,Beresnevichyus, Z. I. G.,Mitskyavichyus, V. Yu.

, p. 1089 - 1095 (2007/10/02)

N-(4-hydroxyphenyl)-β-alanine and its methyl derivatives, as well as p-hydroxy-phenylamino-β,β'-dipropionic acid, were obtained by the reaction of p-aminophenol with methyl acrylate and acrylic, methacrylic, and crotonic acids.The β-alanines were converte

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