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69392-27-4

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69392-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69392-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,9 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69392-27:
(7*6)+(6*9)+(5*3)+(4*9)+(3*2)+(2*2)+(1*7)=164
164 % 10 = 4
So 69392-27-4 is a valid CAS Registry Number.

69392-27-4SDS

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-methyl-6-methylidene-4-prop-1-en-2-ylcyclohexene

1.2 Other means of identification

Product number -
Other names 5-isopropenyl-2-methyl-3-methylene-1-cyclohexene

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:69392-27-4 SDS

69392-27-4Downstream Products

69392-27-4Relevant articles and documents

Development of enantioselective synthetic routes to (-)-Kinamycin F and (-)-lomaiviticin aglycon

Woo, Christina M.,Gholap, Shivajirao L.,Lu, Liang,Kaneko, Miho,Li, Zhenwu,Ravikumar, P. C.,Herzon, Seth B.

, p. 17262 - 17273,12 (2020/09/02)

The development of enantioselective synthetic routes to (-)-kinamycin F (9) and (-)-lomaiviticin aglycon (6) are described. The diazotetrahydrobenzo[b] fluorene (diazofluorene) functional group of the targets was prepared by fluoride-mediated coupling of

MOLYBDENUM CATALYZED ELIMINATIONS OF ALLYLIC ACETATES. NEW DIENE SYNTHESIS

Trost, Barry M.,Lautens, Mark,Peterson, Brian

, p. 4525 - 4528 (2007/10/02)

Allyl acetates smoothly eliminate the elements of acetic acid in the presence of O,N-bis(trimethylsilyl)acetamide and molybdenum hexacarbonyl; a simple sequence permits elaboration of saturated aldehydes into α,β,γ,δ-dienoates which resulted in a four step synthesis of trichonine.

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