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54672-39-8

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54672-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54672-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,7 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54672-39:
(7*5)+(6*4)+(5*6)+(4*7)+(3*2)+(2*3)+(1*9)=138
138 % 10 = 8
So 54672-39-8 is a valid CAS Registry Number.

54672-39-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name exo-2,2-dimethyl-3-methylenebicyclo<2.2.1>heptan-5-ol

1.2 Other means of identification

Product number -
Other names Nojigiku alcohol

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:54672-39-8 SDS

54672-39-8Relevant articles and documents

Electrochemical Oxidation of Polycyclic Cyclopropanes and Camphene. Novel Synthesis of exo-5,5-Dimethyl-6-methylenebicycloheptan-2-ol (Nojigiku Alcohol)

Uchida, Toshikazu,Matsubara, Yoshiharu,Nishiguchi, Ikuzo,Hirashima, Tsuneaki,Ohnishi, Takashi,Kanehira, Koichi

, p. 2938 - 2943 (2007/10/02)

Anodic oxidation of tricyclene (1a) in acetic acid containing triethylamine, followed by hydrolysis, provides a facile and efficient synthesis of exo-5,5-dimethyl-6-methylenebicycloheptan-2-ol (2a), named "nojigiku alcohol", which was isolated from the essential oil of chrysanthemum japonese.Furthermore, a method for large-scale production of 2a starting from the readily available impure starting tricyclene (1a) has been developed by appropriate selection of reaction conditions.Similar electrooxidation of the related naturally occurring polycyclic methylcyclopropanes, cyclofenchene (1b) and longicyclene (1c), followed by hydrolysis also brought about stereo- and regioselective cleavage of carbon-carbon bonds of the cyclopropane rings to give the corresponding homoallylic alcohols 2b,c in good yields.

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