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4,6-bis(hydrazino)-5-nitropyrimidine is a chemical compound with the molecular formula C5H8N8O2. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring with four carbon atoms and two nitrogen atoms. The compound features two hydrazino groups (-NHNH2) attached to the 4 and 6 positions of the pyrimidine ring, and a nitro group (-NO2) at the 5 position. 4,6-bis(hydrazino)-5-nitropyrimidine is known for its potential applications in pharmaceuticals and as a building block in the synthesis of various heterocyclic compounds. Due to its reactivity and the presence of multiple functional groups, it can undergo a variety of chemical reactions, making it a versatile intermediate in organic synthesis.

3856-10-8

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3856-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3856-10-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,5 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3856-10:
(6*3)+(5*8)+(4*5)+(3*6)+(2*1)+(1*0)=98
98 % 10 = 8
So 3856-10-8 is a valid CAS Registry Number.

3856-10-8SDS

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 (6-hydrazinyl-5-nitropyrimidin-4-yl)hydrazine

1.2 Other means of identification

Product number -
Other names 4,6-Dihydrazino-5-nitro-pyrimidin

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:3856-10-8 SDS

3856-10-8Downstream Products

3856-10-8Relevant academic research and scientific papers

4-DIALKYLDITHIOCARBAMOYL-5-NITROPYRIMIDINES. SYNTHESIS, STRUCTURE, PROPERTIES

Makarov, V. A.,Sedov, A. L.,Nemeryuk, M. P.,Solov'ev, N. P.,Anisimova, O. S.,Safonova, T. S.

, p. 1231 - 1234 (1994)

The reaction of 4-chloro-5-nitropyrimidines with sodium dialkyldithiocarbamates gives the corresponding 4-dialkyldithiocarbamoyl derivatives.On heating these derivatives the nitro group is displaced and disulfides are formed at position 5 of the pyrimidine ring.Transformation to 1,3-dithiolopyrimidines has been demonstrated.

New synthetic route to diaminonitropyrazoles as precursors of energetic materials

Guillard, Jér?me,Goujon, Fanny,Badol, Perrine,Poullain, Didier

, p. 5943 - 5945 (2003)

Treatment of nitropyrimidine derivatives with (N-substituted) hydrazines (2 equiv.) gave 1-(substituted)-3,5-diamino-4-nitropyrazole, providing a very mild conversion of pyrimidines into pyrazoles. This reaction provided a convenient route to precursors for new efficient and insensitive explosives.

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