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4-BOC-9-CHLORO-2,3,4,5-TETRAHYDRO-1H-BENZO[E][1,4]DIAZEPINE is a tetrahydrobenzodiazepine derivative featuring a BOC (tert-butoxycarbonyl) protecting group at the 4-position and a chlorine atom at the 9-position. This chemical compound belongs to the benzodiazepine class, known for their sedative, hypnotic, anxiolytic, anticonvulsant, and muscle relaxant properties. The BOC-protecting group is utilized in organic synthesis to shield amine groups, and the chlorine atom may confer unique chemical and biological characteristics to the molecule. As such, 4-BOC-9-CHLORO-2,3,4,5-TETRAHYDRO-1H-BENZO[E][1,4]DIAZEPINE holds promise for applications in medicinal chemistry and drug development.

886364-21-2

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886364-21-2 Usage

Uses

Used in Pharmaceutical Industry:
4-BOC-9-CHLORO-2,3,4,5-TETRAHYDRO-1H-BENZO[E][1,4]DIAZEPINE is used as a precursor in the synthesis of new benzodiazepine-based drugs for the treatment of anxiety, insomnia, and seizure disorders. Its unique structural features, including the BOC-protecting group and the chlorine atom, may enhance the compound's pharmacological properties, such as potency, selectivity, and bioavailability.
Used in Medicinal Chemistry Research:
4-BOC-9-CHLORO-2,3,4,5-TETRAHYDRO-1H-BENZO[E][1,4]DIAZEPINE serves as a valuable research tool in medicinal chemistry for the investigation of structure-activity relationships (SAR) within the benzodiazepine class. By studying the effects of the BOC-protecting group and the chlorine atom on the compound's biological activity, researchers can gain insights into the design of more effective and safer benzodiazepine-based therapeutic agents.
Used in Drug Development:
4-BOC-9-CHLORO-2,3,4,5-TETRAHYDRO-1H-BENZO[E][1,4]DIAZEPINE is employed as a lead compound in drug development programs aimed at discovering novel benzodiazepine-based medications with improved therapeutic profiles. Its unique structural features may offer advantages over existing benzodiazepine drugs, such as reduced side effects, increased selectivity for specific targets, or enhanced pharmacokinetic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 886364-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,6 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 886364-21:
(8*8)+(7*8)+(6*6)+(5*3)+(4*6)+(3*4)+(2*2)+(1*1)=212
212 % 10 = 2
So 886364-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H19ClN2O2/c1-14(2,3)19-13(18)17-8-7-16-12-10(9-17)5-4-6-11(12)15/h4-6,16H,7-9H2,1-3H3

886364-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 9-chloro-1,2,3,5-tetrahydro-1,4-benzodiazepine-4-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 9-chloro-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate

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 -
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More Details:886364-21-2 SDS

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