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46054-87-9

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46054-87-9 Usage

Uses

N-(2-Chlorobenzyl)isopropylamine serves as a reagent in the preparation of new amebicides and also in the preparation of some N-alkyl-N-benzylhaloacetamides. Amecides drugs are used to eradicate the parasitic specie of amebae in animals or humans.

Check Digit Verification of cas no

The CAS Registry Mumber 46054-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,0,5 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 46054-87:
(7*4)+(6*6)+(5*0)+(4*5)+(3*4)+(2*8)+(1*7)=119
119 % 10 = 9
So 46054-87-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H14ClN/c1-8(2)12-7-9-5-3-4-6-10(9)11/h3-6,8,12H,7H2,1-2H3

46054-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2-chlorophenyl)methyl]propan-2-amine

1.2 Other means of identification

Product number -
Other names -

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:46054-87-9 SDS

46054-87-9Relevant articles and documents

Transformation of N,N-diisopropylarylmethylamines into N-isopropylarylmethylamines with molecular iodine

Ezawa, Masatoshi,Moriyama, Katsuhiko,Togo, Hideo

, p. 6689 - 6692 (2016/02/03)

N,N-Diisopropylarylmethylamines were smoothly converted into the corresponding N-isopropylarylmethylamines by the reaction with molecular iodine in the presence of Na2CO3 in chloroform at 60 °C. Other related tertiary amines were also transformed into the corresponding secondary amines by the reaction with molecular iodine under the same reaction conditions.

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