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74209-47-5

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74209-47-5 Usage

Chemical class

Aromatic amines

Molecular weight

304.23 g/mol

Physical state

Colorless to light yellow liquid

Odor

Slightly sweet

Usage

Intermediate in the synthesis of various pharmaceuticals and organic compounds; primarily used in research and development settings

Health hazards

May be harmful if ingested, inhaled, or absorbed through the skin; can cause irritation to the respiratory and digestive systems

Check Digit Verification of cas no

The CAS Registry Mumber 74209-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,0 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74209-47:
(7*7)+(6*4)+(5*2)+(4*0)+(3*9)+(2*4)+(1*7)=125
125 % 10 = 5
So 74209-47-5 is a valid CAS Registry Number.

74209-47-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromophenyl)-2,2-diethoxyethanamine

1.2 Other means of identification

Product number -
Other names Benzeneethanamine,4-bromo-b,b-diethoxy

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:74209-47-5 SDS

74209-47-5Relevant articles and documents

Efficient synthesis of 2-imidazol-2-ylacetates

Ha, Jae Du,Lee, Su Jung,Nam, So Yeun,Kang, Seung Kyu,Cho, Seung Yoon,Ahn, Jin Hee,Choi, Joong-Kwon

, p. 6201 - 6204 (2007/10/03)

A simple method of synthesizing various 2-imidazol-2-ylacetates is described. Condensation of α-aminoketals with imidates, followed by cyclization in refluxing 4 M-HCl/Dioxane, yielded 2-imidazol-2-ylacetates under one-pot and mild reaction conditions.

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