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1,3-DICHLORO-6,7,8,9,10,12-HEXAHYDROAZEPINO[2,1-B]QUINAZOLINE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

149062-75-9

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149062-75-9 Usage

Class

Quinazoline derivative

Dichloro (Cl2)

Two chlorine atoms attached to the molecule

Hexahydro (C6H12)

Six hydrogen atoms attached to a carbon ring

Azepino

Seven-membered nitrogen-containing ring fused to the quinazoline

Structure

A fused ring system consisting of a quinazoline core with a seven-membered nitrogen-containing ring (azepino) attached

Potential Applications

Pharmaceutical industry

Antipsychotic agent

Potential use in treating psychiatric disorders

Research Status

Further research needed to fully understand potential uses and effects

Solubility

Enhanced solubility due to the hydrochloride salt form

Stability

Improved stability due to the hydrochloride salt form

Molecular Weight

Approximately 360.25 g/mol (with hydrochloride)

Appearance

Likely a solid, possibly crystalline, due to the nature of similar compounds

Polarity

Polar, due to the presence of chlorine atoms and the nitrogen-containing ring system

Reactivity

May react with nucleophiles or other reagents capable of reacting with electrophilic centers or functional groups present in the molecule

Check Digit Verification of cas no

The CAS Registry Mumber 149062-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,0,6 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 149062-75:
(8*1)+(7*4)+(6*9)+(5*0)+(4*6)+(3*2)+(2*7)+(1*5)=139
139 % 10 = 9
So 149062-75-9 is a valid CAS Registry Number.

149062-75-9Upstream product

149062-75-9Downstream Products

149062-75-9Relevant academic research and scientific papers

QUINAZOLINE DERIVATIVES AS ACETYLCHOLINESTERASE INHIBITORS

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, (2008/06/13)

A method of treating cognitive deficiencies is described by administering a quinazoline derivative of the general formula wherein A represents in which n is 1-10, P is a bond or (CH2)m in which m is 0-10, and M is =0 , =S , =NR, =CRR, novel compounds of the above are also described as well as methods of manufacture and pharmaceutical compositions.

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