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  • 15284-38-5 Structure
  • Basic information

    1. Product Name: 5-(2-chloroethyl)-2-methyl-2H-tetrazole
    2. Synonyms:
    3. CAS NO:15284-38-5
    4. Molecular Formula: C4H7ClN4
    5. Molecular Weight: 146.5782
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 15284-38-5.mol
    9. Article Data: 1
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 268.9°C at 760 mmHg
    3. Flash Point: 116.4°C
    4. Appearance: N/A
    5. Density: 1.44g/cm3
    6. Vapor Pressure: 0.00749mmHg at 25°C
    7. Refractive Index: 1.626
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-(2-chloroethyl)-2-methyl-2H-tetrazole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-(2-chloroethyl)-2-methyl-2H-tetrazole(15284-38-5)
    12. EPA Substance Registry System: 5-(2-chloroethyl)-2-methyl-2H-tetrazole(15284-38-5)
  • 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: 15284-38-5(Hazardous Substances Data)

15284-38-5 Usage

Description

5-(2-chloroethyl)-2-methyl-2H-tetrazole, commonly referred to as CMET, is a tetrazole derivative characterized by its white crystalline appearance and the molecular formula C5H8ClN5. This chemical compound is recognized for its high reactivity and stability, making it a valuable reagent in organic synthesis and pharmaceutical research. Its potential applications in the medical field, particularly in the development of new drugs and treatment of certain disorders, are of significant interest. However, due to its toxic and hazardous properties, careful handling is required.

Uses

Used in Organic Synthesis:
5-(2-chloroethyl)-2-methyl-2H-tetrazole is used as a reagent in organic synthesis for its high reactivity, facilitating the creation of various heterocyclic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-(2-chloroethyl)-2-methyl-2H-tetrazole is utilized as a building block in the synthesis of new drugs and medicinal compounds, contributing to the development of innovative treatments.
Used in Cancer Treatment Research:
5-(2-chloroethyl)-2-methyl-2H-tetrazole is studied for its potential application in cancer therapy, exploring its effects on tumor growth and the possibility of integrating it into cancer treatment protocols.
Used in Neurological Disorder Research:
CMET is also being investigated for its possible role in the treatment of various neurological disorders, indicating its potential to contribute to advancements in neurology and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 15284-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,8 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15284-38:
(7*1)+(6*5)+(5*2)+(4*8)+(3*4)+(2*3)+(1*8)=105
105 % 10 = 5
So 15284-38-5 is a valid CAS Registry Number.

15284-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-chloroethyl)-2-methyltetrazole

1.2 Other means of identification

Product number -
Other names 5-(2-chloroethyl)-2-methyl-2h-tetrazole

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:15284-38-5 SDS

15284-38-5Synthetic route

5-(2-chloroethyl)-1H-tetrazole
18755-46-9

5-(2-chloroethyl)-1H-tetrazole

methyl iodide
74-88-4

methyl iodide

A

2-methyl-5-(2-chloroethyl)tetrazole
15284-38-5

2-methyl-5-(2-chloroethyl)tetrazole

B

5-(2-Chloro-ethyl)-1-methyl-1H-tetrazole
15284-37-4

5-(2-Chloro-ethyl)-1-methyl-1H-tetrazole

Conditions
ConditionsYield
With triethylamine In acetone Heating; Yield given;
2-methyl-5-(2-chloroethyl)tetrazole
15284-38-5

2-methyl-5-(2-chloroethyl)tetrazole

2-methyl-5-vinyl-2H-tetrazole
15284-39-6

2-methyl-5-vinyl-2H-tetrazole

Conditions
ConditionsYield
With sodium hydroxide In methanol at 35℃;51%

15284-38-5Downstream Products

15284-38-5Relevant articles and documents

SYNTHESIS AND PROPERTIES OF 2-ALKYL-5-ETHYNYLTETRAZOLES

Buzilova, S. R.,Shul'gina, V. M.,Gareev, G. A.,Vereshchagin, L. I.

, p. 658 - 663 (2007/10/02)

2-Alkyl-5-ethynyltetrazoles were synthesized.It is shown that ethynyltetrazoles have a triple bond with increased electrophilicity.They readily add aliphatic alcohols and amines and undergo aminomethylation, the Iotsich reaction, oxidative dimerization, and the cycloaddition of azides. 1-Phenyl-3-tetrazolyl-2-propyne, which has the properties of α-acetylenic ketones, was obtained by selective oxidation of tetrazolylethynylcarbinol.

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