Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1019567-85-1

Post Buying Request

1019567-85-1 Suppliers

Recommended suppliersmore

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

1019567-85-1 Usage

General Description

4-[(1-Phenyl-ethylaMino)-Methyl]-benzonitrilehydrochloride is a chemical compound that is typically found in the form of a white powder. It is commonly used in pharmaceutical research and development as a potential drug candidate for treating various medical conditions. 4-[(1-Phenyl-ethylaMino)-Methyl]-benzonitrilehydrochloride has a molecular formula of C16H15N2? HCl and a molecular weight of 283.77 g/mol. The chemical structure consists of a benzene ring with a nitrile group and an aminoethyl group attached, as well as a methyl group substituted to the amino group. The hydrochloride salt form of this compound makes it more stable and soluble in water, enhancing its bioavailability and potential for use in medicinal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1019567-85-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,9,5,6 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1019567-85:
(9*1)+(8*0)+(7*1)+(6*9)+(5*5)+(4*6)+(3*7)+(2*8)+(1*5)=161
161 % 10 = 1
So 1019567-85-1 is a valid CAS Registry Number.

1019567-85-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(1-phenylethylamino)methyl]benzonitrile,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-(((1-Phenylethyl)amino)methyl)benzonitrile hydrochloride

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:1019567-85-1 SDS

1019567-85-1Downstream Products

1019567-85-1Relevant articles and documents

Synthesis of Enantioenriched Amines by Iron-Catalysed Amination of Alcohols Employing at Least One Achiral Substrate

Bottari, Giovanni,Afanasenko, Anastasiia,Castillo-Garcia, Antonio A.,Feringa, Ben L.,Barta, Katalin

, p. 5436 - 5442 (2021)

The synthesis of a broad range of enantioenriched amines by the direct Fe-catalysed coupling of amines with alcohols through the borrowing hydrogen strategy, while at least one of these substrates is achiral is reported. When starting from α-chiral amines and achiral alcohols, a wide range of enantioenriched amine products, including N-heterocyclic moieties can be obtained with complete retention of stereochemistry and the power of this method is demonstrated in the one-step synthesis of known pharmaceuticals from commercially available, simple enantiopure primary amines and achiral alcohols. It was also found that the use of β-branched enantioenriched primary alcohols and achiral amines as reaction partners leads to a partial loss of stereochemical integrity in the final product, however, a systematic optimization enabled partial retention of enantiopurity and possible parameters effecting for racemization were identified. (Figure presented.).

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

What can I do for you?
Get Best Price

Get Best Price for 1019567-85-1