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Bicyclo[3.2.1]oct-3-en-2-one, 3-chloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51145-45-0

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51145-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51145-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,4 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51145-45:
(7*5)+(6*1)+(5*1)+(4*4)+(3*5)+(2*4)+(1*5)=90
90 % 10 = 0
So 51145-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H9ClO/c9-7-4-5-1-2-6(3-5)8(7)10/h4-6H,1-3H2

51145-45-0SDS

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 3-chlorobicyclo[3.2.1]oct-3-en-2-one

1.2 Other means of identification

Product number -
Other names Chlor-3-bicyclo[3.2.1]octen-3-on-2

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:51145-45-0 SDS

51145-45-0Downstream Products

51145-45-0Relevant academic research and scientific papers

3 - [4 - (methyl sulfonyl) - 2-chlorobenzoyl] bicyclo [3.2.1] - 2,4- octadione method for the synthesis of (by machine translation)

-

, (2016/10/08)

3 - [4 - (methyl sulfonyl) - 2-chlorobenzoyl] bicyclo [3.2.1]-octane -2,4-dione are synthetic intermediates of the herbicide, the present invention discloses a synthetic 3 - [4 - (methyl sulfonyl) - 2-chlorobenzoyl] bicyclo [3.2.1]-octane -2,4-dione metho

Method for producing bicyclic 1,3-diketones

-

, (2008/06/13)

A process for preparing bicyclic 1,3-diketones of the formula I where R1, R2, R3 and R4 are hydrogen, C1-C4-alkyl, C1-C4-alkoxy-carbonyl, halogen, cyano, nitro, C1-C4-alkylthio, C1-C4-alkylsulfenyl or C1-C4-alkylsulfonyl and Z is C1-C4-alkylene, O, S, N—R5 where R5 is C1-C4-alkyl or C1-C4-alkylcarbonyl, which comprises a) reacting a bicyclic olefin of the formula II with haloform in the presence of a base to give the ring-expanded product of the formula III where R1-R4 and Z are as defined above and X is halogen; b) hydrolyzing the allylic halogen of the compound of the formula III to the allyl alcohol of the formula IV c) oxidizing the allyl alcohol of the formula IV to the unsaturated ketone of the formula V d) reacting the ketone of the formula V with a nucleophilic ion Y? which stabilizes a negative charge to give the ketone of the formula VI e) hydrolyzing the ketone of the formula VI to the bicyclic 1,3-diketone of the formula I, novel intermediates and novel processes for preparing these intermediates are described.

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