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1H-1,4-Benzodiazepine, 7-chloro-2,3,4,5-tetrahydro-1-methyl-5-phenyl- is a complex organic compound belonging to the benzodiazepine class. This molecule is characterized by a seven-membered benzene ring fused to a diazepine ring, with a chlorine atom at the 7th position. The compound also features a tetrahydro structure, meaning it contains four hydrogen atoms bonded to carbon atoms in a saturated manner. Additionally, it has a methyl group (CH3) at the 1st position and a phenyl group (C6H5) at the 5th position. This specific chemical structure is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various benzodiazepine-based drugs, which are used to treat anxiety, insomnia, and other central nervous system disorders.

4267-07-6

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4267-07-6 Usage

Chemical class

Benzodiazepine

Structure

1H-1,4-Benzodiazepine, 7-chloro-2,3,4,5-tetrahydro-1-methyl-5-phenyl-

Central nervous system effect

Depressant

Sedative properties

Yes

Hypnotic properties

Yes

Anxiolytic properties

Yes

Muscle relaxant properties

Yes

Common uses

Treatment of anxiety, insomnia, seizures, and muscle spasms

Potential for addiction

Yes

Dependence risk

High

Withdrawal symptoms

Possible

Recommended use

Under the guidance of a healthcare professional

Check Digit Verification of cas no

The CAS Registry Mumber 4267-07-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,6 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4267-07:
(6*4)+(5*2)+(4*6)+(3*7)+(2*0)+(1*7)=86
86 % 10 = 6
So 4267-07-6 is a valid CAS Registry Number.

4267-07-6Downstream Products

4267-07-6Relevant academic research and scientific papers

Process for preparing 1,4-benzodiazepines

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, (2008/06/13)

1,4-Benzodiazepine derivatives of the formula, STR1 wherein R1 is hydrogen, a lower alkyl, a haloalkyl, a cycloalkylalkyl, an alkoxyalkyl, an acyloxyalkyl, an alkylthioalkyl, an alkylaminoalkyl, a dialkylaminoalkyl, a hydroxyalkyl, carbamoyl, or an N-alkylcarbamoyl; R2 is hydrogen or a lower alkyl; X is hydrogen, a halogen, nitro, or trifluoromethyl; A is a group of the formula, STR2 (wherein Y and Z each represent hydrogen, a halogen, a lower alkyl, or nitro) and a salt thereof, are prepared by reacting a 1,4-benzodiazepin-2-one compound of the formula, STR3 wherein R1, R2, X, Y and Z are the same as defined above, with diborane in an inert solvent.

Preparation of benzodiazepines

-

, (2008/06/13)

A 1-alkyl-1,2,4,5-tetrahydro-3H-1,4-benzodiazepine derivative is produced by contacting a 1-aminoethyl-indole derivative with a suitable oxidizing agent and then reducing the resulting 1-acyl-2,3-dihydro-1H-1,4-benzodiazepine derivative. The starting 1-am

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