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67883-68-5

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67883-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67883-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,8 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67883-68:
(7*6)+(6*7)+(5*8)+(4*8)+(3*3)+(2*6)+(1*8)=185
185 % 10 = 5
So 67883-68-5 is a valid CAS Registry Number.

67883-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5-trimethyl-6-prop-2-enylbenzene-1,4-diol

1.2 Other means of identification

Product number -
Other names 2-Allyl-3,5,6-trimethyl-hydrochinon

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:67883-68-5 SDS

67883-68-5Relevant articles and documents

Development of Novel Phenolic Antioxidants. Synthesis, Structure Determination, and Analysis of Spiro

Gilbert, John C.,Pinto, Marian

, p. 5271 - 5276 (2007/10/02)

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Allylation of Quinones with Allyltin Reagents

Naruta, Yoshinori

, p. 3774 - 3783 (2007/10/02)

Lewis acid (BF3) catalyzed allylation of quinones with allyl- (2a), 2-methyl-2-propenyl- (2b), trans-2-butenyl- (2c,d), 3-methyl-2-butenyl- (2e,f), and trans-cinnamyltrialkyltin (2g) gives the corresponding allylhydroquinones with high regioselectivity.Vitamin K2(5) (7) and coenzyme Q1 (9) were prepared in yields of 78 and 75percent, respectively.These reactions appear to proceed through allylquinol intermediates which undergo rearrangement under the influence of BF3.The success of this synthesis of vitamin K2(5) and coenzyme Q1 depends on the fact that the reaction of 3-methyl-2-butenyltin with quinones occurs at the α carbon of the allylic system.

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