Welcome to LookChem.com Sign In|Join Free
  • or
2-Methyl-5-(trifluoromethyl)-2H-tetrazole is a chemical compound with the molecular formula C3H3F3N4. It is a heterocyclic compound, specifically a tetrazole derivative, characterized by the presence of four nitrogen atoms in a ring structure. 2-Methyl-5-(trifluoromethyl)-2H-tetrazole features a methyl group (-CH3) at the 2-position and a trifluoromethyl group (-CF3) at the 5-position. It is known for its stability and reactivity, often used as a reagent in organic synthesis, particularly in the formation of various chemical bonds. Due to its unique properties, it has applications in the pharmaceutical and chemical industries, where it can act as a building block for more complex molecules or as a catalyst in certain reactions.

768-27-4

Post Buying Request

768-27-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

768-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 768-27-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 768-27:
(5*7)+(4*6)+(3*8)+(2*2)+(1*7)=94
94 % 10 = 4
So 768-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H3F3N4/c1-10-8-2(7-9-10)3(4,5)6/h1H3

768-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-5-(trifluoromethyl)tetrazole

1.2 Other means of identification

Product number -
Other names 2-Methyl-5-trifluormethyl-tetrazol

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:768-27-4 SDS

768-27-4Upstream product

768-27-4Downstream Products

768-27-4Relevant academic research and scientific papers

Positional Selectivity of the Methylation of 5-Substituted Tetrazolate Anions

Spear, Robert J.

, p. 2453 - 2468 (2007/10/02)

The methylation of a series of 15 sodium 5-substituted tetrazolates using iodomethane in acetone/water (4:1) has been studied.The reaction yields both 1- and 2-methyl products, and the ratio of these products is discussed in terms of the nature of the 5-substituent.Electronic and steric effects dominate the reaction pathway; both increased substituent electronegativity and steric bulk lead to predominant methylation at N 2.Sodium 5-ethoxycarbonyltetrazolate (3n) goes against this trend and an intermediate is proposed where the incoming electrophile is associated with the ester carbonyl group.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 768-27-4