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Diethyl 2-(1-methyl-1-nitroethyl)butanedioate is a complex organic compound with the chemical formula C11H19NO6. It is a type of ester derived from butanedioic acid (succinic acid) and features a nitro group and a methyl group attached to the ethyl chain. diethyl 2-(1-methyl-1-nitroethyl)butanedioate is characterized by its yellowish color and is soluble in organic solvents. It is synthesized through a series of chemical reactions, often involving the esterification of succinic acid with ethanol and subsequent nitration and alkylation steps. Diethyl 2-(1-methyl-1-nitroethyl)butanedioate has potential applications in the pharmaceutical and chemical industries, particularly as an intermediate in the synthesis of various drugs and other organic compounds. Due to its complex structure and reactivity, it is important to handle this chemical with care, adhering to proper safety protocols.

2088-01-9

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2088-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2088-01-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,8 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2088-01:
(6*2)+(5*0)+(4*8)+(3*8)+(2*0)+(1*1)=69
69 % 10 = 9
So 2088-01-9 is a valid CAS Registry Number.

2088-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (α-nitro-isopropyl)-succinic acid diethyl ester

1.2 Other means of identification

Product number -
Other names 2-(1-methyl-1-nitro-ethyl)-succinic acid diethyl 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:2088-01-9 SDS

2088-01-9Downstream Products

2088-01-9Relevant academic research and scientific papers

PROCESS FOR PREPARING ALKYLIDENE-SUBSTITUTED-1,4-DIONS DERIVATIVES

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Page 15-16, (2008/06/13)

A process for the preparation of a monoalkylidene substituted 1,4-dions derivatives of formula (Ia) or (Ib) or a mixture of (Ia) and (Ib): wherein: R1, R2 and R3, equal to or different from each other, are hydrogen atoms or C1-C20 hydrocarbon groups: T1 and T2, equal to or different from each other, are OR4. R4, NR42, SR4 or PR42; or T1 and T2 can be fused in an oxygen atom or a NR4 group; said process comprises the step of reacting a compound of formula (II), with a compound of formula (IIIa) or (IIIb), in the presence of at least one equivalent with respect to the compound of formula (IIIa) or (IIIb) of a salts of a base or a neutral base at a temperature higher than 70°C.

PROCESS FOR PREPARING ALKYLIDENE-SUBSTITUTED-1,4-DIONS DERIVATIVES

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Page 14-15, (2010/02/06)

A process for the preparation of a monoalkylidene substituted 1,4-dions derivatives of formula (Ia) or (Ib) or a mixture of (Ia) and (Ib): wherein: R1, R2 and R3, equal to or different from each other, are hydrogen atoms or C1-C20 hydrocarbon groups: T1 and T2, equal to or different from each other, are OR4, R4, NR42, SR4 or PR42; or T1 and T2 can be fused in an oxygen atom or a NR4 group; said process comprises the step of reacting a compound of formula (II) with a compound of formula (IIIa) or (IIIb) in the presence of at least one equivalent with respect to the compound of formula (IIIa) or (IIIb) of a carbonate of metal M or of a compound of formula MTj such as K2C03 or KHC03.

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