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490-06-2

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490-06-2 Usage

Uses

3-Isopropyl-6-methylbenzene-1,2-diol is an antioxidant used in food.

Check Digit Verification of cas no

The CAS Registry Mumber 490-06-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 490-06:
(5*4)+(4*9)+(3*0)+(2*0)+(1*6)=62
62 % 10 = 2
So 490-06-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2/c1-6(2)8-5-4-7(3)9(11)10(8)12/h4-6,11-12H,1-3H3

490-06-2SDS

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 3-methyl-6-propan-2-ylbenzene-1,2-diol

1.2 Other means of identification

Product number -
Other names 3-Isopropyl-6-methylpyrocatechol

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:490-06-2 SDS

490-06-2Relevant articles and documents

-

Gray,R.T.,Smith,H.E.

, p. 4229 - 4271 (1967)

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Enantioselective synthesis of bicyclo[2.2.2]octenones using a copper-mediated oxidative dearomatization/[4 + 2] dimerization cascade

Dong, Suwei,Zhu, Jianglong,Porco Jr., John A.

, p. 2738 - 2739 (2008/09/19)

An enantioselective approach to bicyclo[2.2.2]octenone structures utilizing a copper-mediated asymmetric oxidative dearomatization/[4 + 2] dimerization cascade is described. The total synthesis and absolute stereochemistry reassignment of (+)-aquaticol has been achieved using the methodology. Copyright

Regio- and stereoselectivities in Diels-Alder cyclodimerizations of orthoquinonoid cyclohexa-2,4-dienones

Gagnepain, Julien,Méreau, Rapha?l,Dejugnac, Delphine,Léger, Jean-Michel,Castet, Frédéric,Deffieux, Denis,Pouységu, Laurent,Quideau, Stéphane

, p. 6493 - 6505 (2008/02/08)

The [4+2] cyclodimerization of cyclohexa-2,4-dienone derivatives of the orthoquinone monoketal and orthoquinol types has been the topic of numerous investigations over the last 50 years in the aim of rationalizing the extraordinary level of regio-, site-,

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