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2-Nitrobutyl acetate is an organic compound with the chemical formula C6H11NO4. It is a nitrate ester derived from 2-nitrobutane and acetic acid, featuring a nitro group (-NO2) attached to a butyl chain and an acetate group (-OOCCH3). This colorless liquid is used as a solvent and a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential to form explosive compounds, 2-nitrobutyl acetate requires careful handling and storage.

2123-71-9

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2123-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2123-71-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,2 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2123-71:
(6*2)+(5*1)+(4*2)+(3*3)+(2*7)+(1*1)=49
49 % 10 = 9
So 2123-71-9 is a valid CAS Registry Number.

2123-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitrobutyl acetate

1.2 Other means of identification

Product number -
Other names acetic acid 2-nitro-butyl ester

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:2123-71-9 SDS

2123-71-9Relevant academic research and scientific papers

Novel electrophilic ipso acylation - Detosylation reaction of pyrroles

Pelkey, Erin T.,Gribble, Gordon W.

, p. 1338 - 1342 (2007/10/03)

A pyrrole and two pyrroloindoles that are substituted with a p-toluenesulfonyl group undergo an ipso acylation - detosylation reaction with acid chlorides and aluminum chloride to afford the corresponding acyl-substituted pyrroles and pyrroloindoles.

Reaction of 2-Nitroenamines and 2-Nitroalkenyl Sulfides with Ethyl Isocyanoacetate. A Novel Synthesis of 1-Hydroxypyrazoles

Uno, Hidemitsu,Kinoshita, Tomohito,Matsumoto, Koji,Murashima, Takashi,Ogawa, Takuji,Ono, Noboru

, p. 570 - 581 (2007/10/03)

We have show that 1-hydroxypyrazoles can be prepared easily and regioselectively from the reaction of nitroenamines with ethyl isocyanoacetate. α,β-Unsaturated aci-nitronates are formed in the reaction and are then hydrolysed to give the products by quenching with acid.

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