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Bicyclo[4.1.0]heptane-1-carboxylic acid, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92984-25-3

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92984-25-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92984-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,8 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92984-25:
(7*9)+(6*2)+(5*9)+(4*8)+(3*4)+(2*2)+(1*5)=173
173 % 10 = 3
So 92984-25-3 is a valid CAS Registry Number.

92984-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl bicyclo[4.1.0]heptane-6-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:92984-25-3 SDS

92984-25-3Downstream Products

92984-25-3Relevant academic research and scientific papers

Substituent Effects on Hydrogenation of Aromatic Rings: Hydrogenation vs. Hydrogenolysis in Cyclic Analogues of Benzyl Ethers.

Anzalone, Luigi,Hirsch, Jerry A.

, p. 2128 - 2133 (1985)

Carbalkoxy substituents are shown to retard the hydrogenation of aromatic rings over Rh/C catalyst.Hydrogenolysis predominates with acyclic (benzyloxy)acetates over this catalyst, but both hydrogenation and hydrogenolysis become sluggish with 2-isochroman-4-ones (1).However, phthalides may be cleanly hydrogenated in moderate to excellent yields without significant hydrogenolysis.Placing a benzyl ether in a ring system appears to greatly retard hydrogenolysis relative to the acyclic analogues.

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