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9-bromo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72472-29-8

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72472-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72472-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,7 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72472-29:
(7*7)+(6*2)+(5*4)+(4*7)+(3*2)+(2*2)+(1*9)=128
128 % 10 = 8
So 72472-29-8 is a valid CAS Registry Number.

72472-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-bromo-6,7,8,9-tetrahydrobenzo[7]annulen-5-one

1.2 Other means of identification

Product number -
Other names 9-bromo-6,7,8,9-tetrahydrobenzocyclohepten-5-one

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:72472-29-8 SDS

72472-29-8Upstream product

72472-29-8Downstream Products

72472-29-8Relevant academic research and scientific papers

Generation of cycloheptynes and cyclooctynes via a sulfoxide-magnesium exchange reaction of readily synthesized 2-sulfinylcycloalkenyl triflates

Yoshida, Suguru,Karaki, Fumika,Uchida, Keisuke,Hosoya, Takamitsu

supporting information, p. 8745 - 8748 (2015/05/20)

Cycloheptynes and cyclooctynes were efficiently generated via a sulfoxide-magnesium exchange reaction of readily synthesized 2-sulfinylcycloalkenyl triflates. Cycloadditions between various ynophiles and the cycloalkynes generated by this method proceeded

Tetrahydrobenzindole derivatives

-

, (2008/06/13)

Compounds containing tetrahydrobenzindole which bind to serotonin receptor and are useful in treatment or prevention of disease induced by abnormality of central peripheral serotonin controlling functions.

General Photoisomerization Approach to trans-Benzobicyclooctenes: Synthetic and Mechanistic Studies

Smith, Amos B.,Wood, John L.,Keenan, Terence P.,Liverton, Nigel,Visnick, Melean

, p. 6652 - 6666 (2007/10/02)

The preparation and photoisomerization of cis-bicyclooctenes (+)-3, 16, and 21-23 are described.For the benzannulated substrates, the primary photochemical events established photostationary states between the cis isomers and the trans-fused cyclop

Bridged-ring Nitrogen Compounds. Part 7. Synthesis of the 1,4-Ethano-3-benzazepine Ring System

Sedgeworth, Janette,Proctor, George R.

, p. 2677 - 2688 (2007/10/02)

9-Bromobenzosuberone was converted via 9-cyanobenzosuberone into several other 9-substituted benzosuberones, but attemps to cause them to cyclise to the tricyclic 1,4-ethano-3-benzazepine ring system were unsuccessful.Both ethyl phenylacetate and ethyl 3-methoxyphenylacetate were converted by conventional procedures into the corresponding 6,7,8,9-tetrahydro-5-methyl-9,10-dioxo-5,8-methano-5H-benzocycloheptenes.The 3-methoxy derivative was further converted into N-benzyl-8-bromo-6,7,8,9-tertrahydro-3-methoxy-5-methyl-9-oxo-5H-benzocycloheptene-5-carboxamide which could be converted into the tricyclic 3-benzyl-2,3,4,5-tetrahydro-8-methoxy-1-methyl-2,5-dioxo-1,4-ethano-1H-3-benzazepine and thence in two steps into both 3-benzyl-2,3,4,5-tetrahydro-8-methoxy-1-methyl-1,4-ethano-1H-3-benzazepine and 3-benzyl-2,3,4,5-tetrahydro-8-hydroxy-1-methyl-1,4-ethano-1H-3-benzazepine.Also prepared were 3-benzyl-2,3,4,5-tetrahydro-5-hydroxy-8-methoxy-1-methyl-1,4-ethano-1H-3-benzazepine and 3-benzyl-3,4-dihydro-8-methoxy-1-methyl-1,4-ethano-1H-3-benzazepin-5(2H)-one.

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