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3349-70-0

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3349-70-0 Usage

Chemical structure

A hydrazine derivative containing a cyclobutylidene group and a 2,4-dinitrophenyl group

Application

Used in organic synthesis and pharmaceutical research

Reactivity

Known to have significant reactivity

Usage

Used as a reagent in the preparation of various organic compounds

Potential uses

Interesting compound for further study and application in various fields of science and technology

Check Digit Verification of cas no

The CAS Registry Mumber 3349-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,4 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3349-70:
(6*3)+(5*3)+(4*4)+(3*9)+(2*7)+(1*0)=90
90 % 10 = 0
So 3349-70-0 is a valid CAS Registry Number.

3349-70-0SDS

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 N-(cyclobutylideneamino)-2,4-dinitroaniline

1.2 Other means of identification

Product number -
Other names cyclobutanon-(2,4-dinitro-phenylhydrazone)

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:3349-70-0 SDS

3349-70-0Downstream Products

3349-70-0Relevant articles and documents

A Versatile Synthesis of Four-, Five-, and Six-membered Cyclic Ketones Using Methyl Methylthiomethyl Sulfoxide

Ogura, K.,Yamashita, M.,Suzuki, M.,Furukawa, S.,Tsuchinashi, G.

, p. 1637 - 1642 (2007/10/02)

Cyclization of 1,n-dihaloalkanes with methyl methylthiomethyl sulfoxide in the presence of a base (n-BuLi or KH) gave three-, four-, five-, and six-membered 1-methylsulfinyl-1-methylthiocycloalkanes.These cyclization products were easily converted to the corresponding ketones by acid hydrolysis except 1-methylsulfinyl-1-methylthiocyclopropane which afforded a complicated mixture.The combination of the cyclization with the acidhydrolysis thus provides a new method for synthesizing four-, five-, and six-membered cycloalkanones.Several representative preparations, such as those of substituted cyclobutanones, 3-cyclopentanone, and tetrahydro-4-pyrone are described.

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