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2-methyl-3-nitroprop-1-ene is a chemical compound with the molecular formula C4H7NO2. It is an organic molecule characterized by a propene backbone, which is a three-carbon chain with a double bond between the first and second carbon atoms. The "2-methyl" part of the name indicates that there is a methyl group (a single carbon atom bonded to three hydrogen atoms) attached to the second carbon of the propene chain. The "3-nitro" portion signifies the presence of a nitro group (a nitrogen atom double-bonded to an oxygen atom and single-bonded to another oxygen atom) attached to the third carbon. 2-methyl-3-nitroprop-1-ene is a derivative of propene with a methyl group and a nitro group, which can be used in the synthesis of various organic compounds and has potential applications in the chemical industry.

1606-31-1

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1606-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1606-31-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1606-31:
(6*1)+(5*6)+(4*0)+(3*6)+(2*3)+(1*1)=61
61 % 10 = 1
So 1606-31-1 is a valid CAS Registry Number.

1606-31-1SDS

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 2-methyl-3-nitroprop-1-ene

1.2 Other means of identification

Product number -
Other names 1-Nitro-2-methyl propene

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:1606-31-1 SDS

1606-31-1Relevant academic research and scientific papers

Desilylative Nitration of Alkyl- and Allylsilanes with Nitronium Salts

Olah, George A.,Rochin, Christophe

, p. 701 - 702 (2007/10/02)

Desilylative nitration of methyl- and ethylsilanes with nitronium tetrafluoroborate in sulfolane solution gives nitromethane and nitroethane, respectively.Higher alkylsilanes are also nitrated, but the reactions are followed by HNO2 elimination.The method represents the first successful nitrodesilylations at saturated carbon.Allylsilanes react cleanaly with NO2BF4 in methylene chloride solution to give nitropropanes in good to excellent yield.These reactions, however, involve initial attack by NO2+ on the allylic ?-system followed by fluoride-induced trimethylsilyl elimination and not direct desilylative nitration at saturated carbon. 1-(Trimethylsilyl)but-2-ene gives exclusive secondary 3-nitrobut-1-ene and not the primary direct nitrodesilylation product 1-nitrobut-2-ene.

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