Welcome to LookChem.com Sign In|Join Free

CAS

  • or

7171-70-2

1,3,5-trimethyl-4-nitroso-1H-pyrazole is a chemical compound with the molecular formula C6H10N4O. It is a derivative of pyrazole, a heterocyclic compound consisting of a five-membered ring with two nitrogen atoms and three carbon atoms. In this specific compound, three methyl groups (CH3) are attached to the 1st, 3rd, and 5th positions of the pyrazole ring, and a nitroso group (NO) is present at the 4th position. 1,3,5-trimethyl-4-nitroso-1H-pyrazole is known for its potential applications in various chemical and pharmaceutical industries, such as in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Due to its unique structure and properties, it can also be used as an intermediate in the preparation of other complex molecules.

7171-70-2

Post Buying Request

7171-70-2 Suppliers

Recommended suppliersmore

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

7171-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7171-70-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7171-70:
(6*7)+(5*1)+(4*7)+(3*1)+(2*7)+(1*0)=92
92 % 10 = 2
So 7171-70-2 is a valid CAS Registry Number.

7171-70-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-Trimethyl-4-nitroso-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 4H-1,2,6-Thiadiazin-4-one,3,5-diamino-,oxime,1,1-dioxide

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:7171-70-2 SDS

7171-70-2Relevant articles and documents

Experimental standard molar enthalpies of formation of crystalline 3,5-dimethylpyrazole, 3,5-dimethyl-4-nitrosopyrazole, 1,3,5-trimethyl-4-nitrosopyrazole, and 3,5-dimethyl-1-phenyl-4-nitrosopyrazole

Ribeiro da Silva, Maria D.M.C.,Ferreira, Susana C.C.,Rodrigues, Ivone A.P.,Da Silva, Luis C.M.,Acree Jr, William E.,Pandey, Siddharth,Roy, Lindsay E.

, p. 1227 - 1235 (2007/10/03)

Static-bomb calorimetry was used to measure standard molar enthalpies of combustion in oxygen for crystalline compounds. The standard molar enthalpies of formation of the crystalline compounds were derived using the measured values. The values of the stan

Reactions of pyrazoles and pyrazolium salts with complex metal hydrides and organometallic reagents. Synthesis of pyrazolines and pyrazolidines

Cuadrado, Purificacion,Gonzalez-Nogal, Ana M.,Martinez, Senen

, p. 8585 - 8598 (2007/10/03)

2-Pyrazolin-4-oximes have been synthesized by reaction of 4-nitroso- and 4-nitropyrazoles with complex metal hydrides and organometallic reagents. Furthermore, 4-nitropyrazolium tetrafluoroborates are reactive substrates towards organolithium and Grignard

Studies in nitrosopyrazoles. Part 1. Preparative and spectroscopic studies of some 3,5-dialkyl-4-nitrosopyrazoles

Cameron, Mailer,Gowenlock, Brian G.,Boyd, Alan S. F.

, p. 2271 - 2274 (2007/10/03)

The preparations of a number of 3,5-disubstituted- and 1,3,5-trisubstituted-4-nitrosopyrazoles are described and a range of physical properties of these compounds are measured. Comparison is made with some 2,6-disubstituted nitrosobenzenes and it is shown from 13C NMR spectroscopy that the effects of substitution by flanking tert-butyl groups are moderated in the case of the pyrazoles from those in the aromatic C6 ring due to a lessening of steric hindrance. It is also suggested that steric effects are evident in the preparation of 1,3,5-substituted-4-nitrosopyrazoles when one of the flanking groups to the NO is tert-butyl or phenyl, there being no such effect for the corresponding case of the isobutyl 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

What can I do for you?
Get Best Price

Get Best Price for 7171-70-2