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90095-71-9

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90095-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90095-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,9 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90095-71:
(7*9)+(6*0)+(5*0)+(4*9)+(3*5)+(2*7)+(1*1)=129
129 % 10 = 9
So 90095-71-9 is a valid CAS Registry Number.

90095-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-1,3-bis(trifluoroacetoxy)-1,3-diphenylpropane

1.2 Other means of identification

Product number -
Other names Trifluoro-acetic acid (1R,3R)-1,3-diphenyl-3-(2,2,2-trifluoro-acetoxy)-propyl 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:90095-71-9 SDS

90095-71-9Downstream Products

90095-71-9Relevant articles and documents

TRANSFORMATIONS OF PHENYLCYCLOPROPANES UNDER THE INFLUENCE OF VARIOUS DIACYLOXYIODO DERIVATIVES

Saginova, L. G.,Bondarenko, O. B.,Gazzaeva, R. A.,Shabarov, Yu. S.

, p. 477 - 480 (2007/10/02)

The reaction of phenylcyclopropanes with various (diacycloxyiodo)benzenes and iodine tristrifluoracetate was studied. (Bistrichloroacetoxyiodo)benzene and (bistrifluoracetoxyiodo)benzene react with phenylcyclopropanes exclusively in the small ring with the formation of the respective 1-phenyl-1,3-bis(acyloxy)propanes.Iodine tristrifluoroacetate in reaction with phenylcyclopropanes attacks both the small ring and the aromatic ring, which leads to the production of the esters of 1,3-diols and p-iodophenylcyclopropanes.Possible mechanisms are proposed for the oxidative cleavage of the trimethyl ring of phenylcyclopropanes.

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