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1,4-Dihydro-9-isopropylidene-1,4-methano-naphthalene, also known as 9-isopropyl-1,4-methanonaphthalene, is a chemical compound with the molecular formula C13H14. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. 1,4-DIHYDRO-9-ISOPROPYLIDENE-1,4-METHANO-NAPHTHALENE, 99 is characterized by its unique structure, which includes a naphthalene core with a methyl bridge (methano) connecting the two aromatic rings, an isopropyl group attached to one of the carbons, and a dihydro functional group indicating the presence of two hydrogen atoms. It is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties. The compound is typically synthesized through various chemical reactions and is subject to strict quality control, with a purity level of 99% being a common standard in the industry.

7350-72-3

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7350-72-3 Usage

Type of Compound

Cyclic compound

Purity

99%

Industry Usage

Pharmaceutical industry

Application

Building block for the synthesis of various drugs and chemical compounds

Role in Organic Synthesis

Precursor to other chemical compounds

Starting Material

Preparation of complex molecules

Field of Importance

Organic chemistry

Availability

Widely used and considered versatile

Check Digit Verification of cas no

The CAS Registry Mumber 7350-72-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7350-72:
(6*7)+(5*3)+(4*5)+(3*0)+(2*7)+(1*2)=93
93 % 10 = 3
So 7350-72-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H14/c1-9(2)14-12-7-8-13(14)11-6-4-3-5-10(11)12/h3-8,12-13H,1-2H3

7350-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-isopropylidene-cis-tricyclo[6,2,1,02,7]undeca-2,4,6,9-tetraene

1.2 Other means of identification

Product number -
Other names 9-isopropylidene-1,4-dihydro-1,4-methanonaphthalene

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:7350-72-3 SDS

7350-72-3Relevant academic research and scientific papers

The Dechlorination of Some Highly Chlorinated Naphthalene Derivatives

Hales, Neil J.,Heaney, Harry,Hollinshead, John H.,Lai, Steven M. F.,Singh, Pritpal

, p. 7777 - 7790 (2007/10/02)

The cycloadducts formed between tetrachlorobenzyne and a variety of arenes and cyclic 1,3-dienes have been reductively dechlorinated.The products are formally benzyne cycloadducts, many of which are difficult to make by other routes.High yields are obtained when sodium and t-butanol in boiling THF are used for the reduction.THF serves as a solvent but t-butanol not only acts as a proton donor but also appears to initiate the reduction.Tetrachlorobenzyne should be considered as an alternative reagent whenever benzyne itself appears to be required.

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