Welcome to LookChem.com Sign In|Join Free

CAS

  • or

7074-00-2

Post Buying Request

7074-00-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7074-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7074-00-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7074-00:
(6*7)+(5*0)+(4*7)+(3*4)+(2*0)+(1*0)=82
82 % 10 = 2
So 7074-00-2 is a valid CAS Registry Number.

7074-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylpropan-2-yl benzenecarboperoxoate

1.2 Other means of identification

Product number -
Other names peroxybenzoic acid-(1-methyl-1-phenyl-ethyl ester)

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:7074-00-2 SDS

7074-00-2Relevant articles and documents

The synthesis of organic peresters via the phase transfer catalysis

Baj,Chrobok

, p. 1185 - 1189 (2007/10/03)

The acylation of alkyl hydroperoxides with acid chlorides under the phase transfer conditions (PTC) is studied. An evident catalytic effect was observed. This reaction can be considered as a convenient method for the synthesis of organic peresters.

DECOMPOSITION HETEROLITIQUE DE PERCARBONATES DE O,O-METHYL-1 PHENYL-1 ETHYLE ET O-ALKYLE OU O-VINYLE EN SOLUTION

Villenave, J. J.,Filliatre, C.,Maillard, B.,Jaouhari, R.

, p. 301 - 310 (2007/10/02)

O,O-α-cumyl O-ethyl, O-vinyl and O-isopropenyl peroxycarbonates (percarbonates) have been prepared from the corresponding chloroformates.Their decompositions have been studied in triisopropylbenzene and di-n-butyl phtalate as solvents; in both cases the main process was the heterolysis of the peroxydic bond (Criegee rearrangement) which gave 2-phenoxy propene.Kinetic studies have been performed using Differential Scanning Microcalorimetry; they have shown that the decomposition of O,O-α-cumyl O-ethyl percarbonate is faster in di-butyl phtalate than in triisopropylbenzene and that the rate constants depend on the initial concentrations of the solutions.From both chemical and kinetic data it has been concluded that the studied percarbonates cannot act as free radical initiators even in non polar media.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 7074-00-2