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(4-methoxy-benzyl)-methyl-phenethyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

302910-90-3

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302910-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 302910-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,9,1 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 302910-90:
(8*3)+(7*0)+(6*2)+(5*9)+(4*1)+(3*0)+(2*9)+(1*0)=103
103 % 10 = 3
So 302910-90-3 is a valid CAS Registry Number.

302910-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxy-benzyl)-methyl-phenethyl-amine

1.2 Other means of identification

Product number -
Other names (4-Methoxy-benzyl)-methyl-phenaethyl-amin

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:302910-90-3 SDS

302910-90-3Relevant academic research and scientific papers

Efficient synthesis of tertiary amines from secondary amines

Kurosu, Michio,Dey, Sevendu Sekhar,Crick, Dean C.

, p. 4871 - 4875 (2007/10/03)

Reliable N-alkylations of secondary amines have been developed. By using DIAD and TPP (or PS-TPP) a variety of secondary amines can be converted to the corresponding tertiary amines in good to excellent yields with diverse alkylhalides; no formation of quaternary amine salts are observed. These protocols are amenable to combinatorial chemistry libraries, and are also useful for the syntheses of secondary amines by an acid lysis of the cleavable tertiary amino resins.

Solid-phase synthesis of tertiary methylamines via reductive alkylation-fragmentation using a hydroxylamine linker

Blaney,Grigg,Rankovic,Thoroughgood

, p. 6635 - 6638 (2007/10/03)

The solid-phase synthesis of tertiary methylamines via reductive alkylation-fragmentation employing a hydroxylamine linker is described. The hydroxylamine linker is traceless, robust and versatile, allowing strong organometallic reagents to be used in the synthesis of diverse tertiary methylamines. (C) 2000 Elsevier Science Ltd.

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