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CAS

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3861-76-5

Clonitazene is a synthetic chemical compound belonging to the benzodiazepine class, which is primarily used as a tranquilizer and sedative in veterinary medicine. It is structurally similar to other benzodiazepines such as diazepam and clonazepam, and it works by enhancing the effect of the neurotransmitter gamma-aminobutyric acid (GABA) in the central nervous system, leading to a calming effect. Clonitazene is not approved for human use and is mainly prescribed for animals to manage anxiety, stress, and seizures. Due to its potential for abuse and dependence, it is important to use clonitazene responsibly and under the guidance of a veterinarian.

3861-76-5

3861-76-5 Suppliers

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3861-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3861-76-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,6 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3861-76:
(6*3)+(5*8)+(4*6)+(3*1)+(2*7)+(1*6)=105
105 % 10 = 5
So 3861-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H23ClN4O2/c1-3-23(4-2)11-12-24-19-10-9-17(25(26)27)14-18(19)22-20(24)13-15-5-7-16(21)8-6-15/h5-10,14H,3-4,11-13H2,1-2H3

3861-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[(4-chlorophenyl)methyl]-5-nitrobenzimidazol-1-yl]-N,N-diethylethanamine

1.2 Other means of identification

Product number -
Other names 2-(4-chloro-benzyl)-1-(2-diethylamino-ethyl)-5-nitro-1H-benzimidazole

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:3861-76-5 SDS

3861-76-5Relevant articles and documents

Synthesis, Chemical Characterization, and μ-Opioid Receptor Activity Assessment of the Emerging Group of "nitazene" 2-Benzylbenzimidazole Synthetic Opioids

Vandeputte, Marthe M.,Van Uytfanghe, Katleen,Layle, Nathan K.,St. Germaine, Danielle M.,Iula, Donna M.,Stove, Christophe P.

, p. 1241 - 1251 (2021/05/07)

Several 2-benzylbenzimidazole opioids (also referred to as "nitazenes") recently emerged on the illicit market. The most frequently encountered member, isotonitazene, has been identified in multiple fatalities since its appearance in 2019. Although recent

Synthesis and molecular docking for antiinflammatory studies of 2-(arylmethyl)-1-ethyl-1H-benzo[d]imidazol-5-amines

Bucha, Mallaiah,Eppakayala, Laxminarayana,Malothu, Ramesh,Kudle, Karunakar Rao,Merugu, Ramchander

, p. 29 - 33 (2017/12/15)

1-Chloro-2,4-dinitrobenzene (1) was reacted with aliphatic amines (2) in ethanol as solvent under reflux condition for 16-24 h to form N-alkyl-2,4-dinitroaniline (3). Compound 3 undergoes reduction to from N-alkyl-4-nitrobenzene-1,2-diamine (4). Compound 4 was treated with carboxylic acid (5) to offered N-(2-(alkylamino)-5-nitrophenyl)-2-arylacetamide (6) which on cyclization gave 2-(arylmethyl)-1-ethyl-5-nitro-1H-benzo[d]imidazole (7). Finally, compound 7 undergoes reduction give 2-(arylmethyl)-1-ethyl-1H-benzo[d]imidazol-5-amine (8). The synthesized compounds were characterized by using spectral analyses. The compounds synthesized were confirmed by spectral analyses. Molecular docking of 5COX with the ligand using docking server, predicted the compound to be a potential anti-inflammatory compound.