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87578-93-6

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87578-93-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87578-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,7 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87578-93:
(7*8)+(6*7)+(5*5)+(4*7)+(3*8)+(2*9)+(1*3)=196
196 % 10 = 6
So 87578-93-6 is a valid CAS Registry Number.

87578-93-6SDS

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-(4-methyl-5-oxocyclohex-3-en-1-yl)propan-2-yl acetate

1.2 Other means of identification

Product number -
Other names 1-methyl-1-(4-methyl-5-oxocyclohex-3-enyl)ethyl acetate

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:87578-93-6 SDS

87578-93-6Downstream Products

87578-93-6Relevant articles and documents

Chromium (VI) adsorbed on SiO2/ZrO2, a new supported reagent for allylic oxidations

Baptistella, Lucia H. B.,Sousa, Ilza M. O.,Gushikem, Yoshitaka,Aleixo, Adriana M.

, p. 2695 - 2698 (2007/10/03)

Zirconium (IV) oxide coated on the surface of silica gel was used to absorb Cr(VI) from acidic solutions. This material, in conjunction with t- butyl hydroperoxide, proved to be very useful for allylic oxidations, promoting very clean reactions, with high regioselectivity.

THE STEREOSPECIFIC HYDROXILATION OF ENDOCYCLIC ETHYLENIC LINKAGE IN THE BIOTRANSFORMATION OF α- TERPINYL ACETATE WITH CULTURED SUSPENSION CELLS OF NICOTIANA TABACUM

Hirata, Toshifumi,Lee, Ym Sook,Suga, Takayuki

, p. 671 - 674 (2007/10/02)

The biotransformation of (+/-)-8-acetoxy-p-menth-1-ene (α-terpinyl acetate) with the cultured cells of Nicotiana tabacum was found to result in the predominant formation of 8-acetoxy-c-4-p-menthane-r-1, t-2-diol.This experimental result indicates that the hydroxylation of the endocyclic ethylenic linkage with the cultured suspension cells is stereospecific.

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