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1-Benzyl-5-chloromethyl-1H-[1,2,4]triazole is a triazole derivative with the molecular formula C9H8ClN3. It is a chemical compound that features a five-membered heterocyclic ring with three nitrogen atoms. This versatile compound is widely recognized for its potential applications across various fields, including pharmaceuticals, agrochemicals, and materials science, due to its antifungal and antimicrobial properties.

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  • 885280-92-2 Structure
  • Basic information

    1. Product Name: 1-BENZYL-5-CHLOROMETHYL-1H-[1,2,4]TRIAZOLE
    2. Synonyms: 3-chloromethyl-2-benzyl-1,2,4-triazole
    3. CAS NO:885280-92-2
    4. Molecular Formula: C10H10ClN3
    5. Molecular Weight: 207.66
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 885280-92-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-BENZYL-5-CHLOROMETHYL-1H-[1,2,4]TRIAZOLE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-BENZYL-5-CHLOROMETHYL-1H-[1,2,4]TRIAZOLE(885280-92-2)
    11. EPA Substance Registry System: 1-BENZYL-5-CHLOROMETHYL-1H-[1,2,4]TRIAZOLE(885280-92-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 885280-92-2(Hazardous Substances Data)

885280-92-2 Usage

Uses

Used in Pharmaceutical Industry:
1-Benzyl-5-chloromethyl-1H-[1,2,4]triazole serves as a crucial building block in the synthesis of various pharmaceuticals. Its antifungal and antimicrobial properties make it a valuable component in the development of new drugs targeting a range of infections and diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 1-benzyl-5-chloromethyl-1H-[1,2,4]triazole is utilized for its ability to combat fungal and microbial threats to crops. This application helps in the development of more effective agricultural products that protect plants and enhance overall crop yield.
Used in Materials Science:
1-Benzyl-5-chloromethyl-1H-[1,2,4]triazole also finds potential applications in materials science. Its unique chemical structure allows it to be incorporated into the design and synthesis of advanced materials for various industrial processes, thereby contributing to the development of innovative solutions in this field.

Check Digit Verification of cas no

The CAS Registry Mumber 885280-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,8 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 885280-92:
(8*8)+(7*8)+(6*5)+(5*2)+(4*8)+(3*0)+(2*9)+(1*2)=212
212 % 10 = 2
So 885280-92-2 is a valid CAS Registry Number.

885280-92-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-5-(chloromethyl)-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 3-chloromethyl-2-benzyl-1,2,4-triazole

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:885280-92-2 SDS

885280-92-2Upstream product

885280-92-2Downstream Products

885280-92-2Relevant articles and documents

PHARMACOLOGICALLY ACTIVE GUANIDINE COMPOUNDS

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, (2008/06/13)

The compounds are substituted thioalkyl-, aminoalkyl-and oxyalkyl-guanidines which are inhibitors of histamine activity.

PHARMACOLOGICALLY ACTIVE THIOUREA AND UREA COMPOUNDS

-

, (2008/06/13)

The compounds are substituted thioalkyl-, aminoalkyl-and oxyalkyl-thioureas and ureas which are inhibitors of histamine activity.

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