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19221-36-4

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19221-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19221-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,2 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19221-36:
(7*1)+(6*9)+(5*2)+(4*2)+(3*1)+(2*3)+(1*6)=94
94 % 10 = 4
So 19221-36-4 is a valid CAS Registry Number.

19221-36-4SDS

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 2,2-dichloro-3,4-dihydronaphthalen-1-one

1.2 Other means of identification

Product number -
Other names 2,2-dichloro-3,4-dihydro-2H-naphthalen-1-one

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:19221-36-4 SDS

19221-36-4Relevant articles and documents

-

Stevens et al.

, p. 4590,4592 (1955)

-

The α-Chlorination of Aryl Ketones with Manganese(III) Acetate in the presence of Chloride Ion

Tsuruta, Takehiko,Harada, Tetsuya,Nishino, Hiroshi,Kurosawa, Kazu

, p. 142 - 145 (2007/10/02)

The reaction of 2-(4-methoxyphenyl)-4-chromanone with Mn(OAc)3 in the presence of LiCl gave 3,3-dichloro-2-(4-methoxyphenyl)-4-chromanone.The reactions of 2-phenyl-4-chromanone, 1-phenyl-1-propanone, 1,2-diphenylethanone, and 1-tetralone similarly yielded α,α-dichloro derivatives in good yields. 2,2,2-Trichloroacetophenones were obtained from 2,2-dichloroacetophenones, but in the absence of LiCl, 2,2-dichloroacetophenones gave 2,2,3,3-tetrachloro-1,4-butanediones.KCl, NaCl, NH4Cl,AlCl3, and CaCl2 were also employed as the Cl- ion source.Synthetic applicability and the reaction mechanisms are discussed briefly.

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