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4'-CHLORO-3,3-DIMETHYLBUTYROPHENONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60851-32-3

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60851-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60851-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,5 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60851-32:
(7*6)+(6*0)+(5*8)+(4*5)+(3*1)+(2*3)+(1*2)=113
113 % 10 = 3
So 60851-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H15ClO/c1-12(2,3)8-11(14)9-4-6-10(13)7-5-9/h4-7H,8H2,1-3H3

60851-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)-3,3-dimethylbutan-1-one

1.2 Other means of identification

Product number -
Other names 4-(neopentylcarbonyl)-chlorobenzene

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:60851-32-3 SDS

60851-32-3Relevant academic research and scientific papers

Preparation of unsymmetrical ketones from tosylhydrazones and aromatic aldehydes via formyl C-H bond insertion

Allwood, Daniel M.,Blakemore, David C.,Ley, Steven V.

supporting information, p. 3064 - 3067 (2014/06/23)

Preparation of ketones by insertion of diazo compounds into the formyl C-H bond of an aldehyde is an attractive procedure, but use of structurally diverse diazo compounds is hampered by preparation and safety issues. A convenient procedure for the synthesis of unsymmetrical ketones from bench-stable tosylhydrazones and aryl aldehydes is reported. The procedure can be performed in one pot from the parent carbonyl compound and needs only a base, with no additional promoters being required.

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