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Benzenemethanamine, 3-chloro-N-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90389-47-2

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90389-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90389-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,8 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90389-47:
(7*9)+(6*0)+(5*3)+(4*8)+(3*9)+(2*4)+(1*7)=152
152 % 10 = 2
So 90389-47-2 is a valid CAS Registry Number.

90389-47-2SDS

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 (3-Chloro-benzyl)-ethyl-amine; hydrochloride

1.2 Other means of identification

Product number -
Other names N-ETHYL-M-CHLOROBENZYLAMINE 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:90389-47-2 SDS

90389-47-2Upstream product

90389-47-2Downstream Products

90389-47-2Relevant academic research and scientific papers

Method for preparing amine compound by reducing amide compound

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Paragraph 0155-0157, (2021/02/10)

The invention relates to a method for preparing an amine compound by reducing an amide compound, which comprises the following steps: in a protective atmosphere, mixing the amide compound or cyclic amide, a zirconium metal catalyst and pinacol borane, carrying out amide reduction reaction at room temperature, and carrying out aftertreatment by using an ether solution of hydrogen chloride after 12-48 hours to obtain an amine hydrochloride compound. The method is simple to operate, low in cost, good in functional group tolerance and wide in substrate range.

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