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Benzenepropanoic acid, β-chloro-3-nitro-α-oxo-, methyl ester is a complex organic compound with the chemical formula C10H9ClNO4. It is derived from benzenepropanoic acid, a type of aromatic carboxylic acid, and features a β-chloro substitution, a 3-nitro group, and an α-oxo (keto) functional group. The methyl ester indicates that the carboxylic acid group has been esterified with methanol, resulting in a methyl ester functional group. Benzenepropanoic acid, b-chloro-3-nitro-a-oxo-, methyl ester is characterized by its potential reactivity and may be used in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structural features.

146736-30-3

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146736-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146736-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,7,3 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 146736-30:
(8*1)+(7*4)+(6*6)+(5*7)+(4*3)+(3*6)+(2*3)+(1*0)=143
143 % 10 = 3
So 146736-30-3 is a valid CAS Registry Number.

146736-30-3Relevant academic research and scientific papers

2-AZA-BICYCLO[3.3.0]OCTANE DERIVATIVES

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Page/Page column 11, (2011/02/15)

The invention relates to 2-aza-bicyclo[3.3.0]octane derivatives of Formula (I) wherein A, B, and R1 are as described in the description, and to the use of such compounds, or of pharmaceutically acceptable salts of such compounds, as medicaments, especially as orexin receptor antagonists.

TRANS-3-AZA-BICYCLO[3.1.0]HEXANE DERIVATIVES

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Page/Page column 50; 52, (2009/03/07)

The invention relates to novel trans-3-aza-bicyclo[3.1.0]hexane derivatives of formula (I), wherein A, B, n and R1 are as described in the description, and to the use of such compounds, or of pharmaceutically acceptable salts of such compounds, as medicaments, especially as orexin receptor antagonists.

Substituted benzaldehydes in the darzens condensation with alkyl dihaloacetates

Mamedov,Berdnikov,Tsuboi,Hamamoto,Komiyama,Gorbunova,Gubaidullin,Litvinov

, p. 1455 - 1463 (2007/10/03)

The Darzens reaction of dihaloacetic acid esters with aromatic aldehydes produces either arylhaloglycidic or arylhalopyruvic esters depending on the nature of the substituent in the aromatic ring. Alkyl p- methoxyphenylchloropyruvates undergo spontaneous intermolecular cyclocondensation to form pyranone or furanone derivatives depending on the character of the alkyl fragment.

CONDENSATION OF METHYL 2-CHLORO-3-(3-NITROPHENYL)-2,3-EPOXYPROPIONATE WITH 1,2-PHENYLENE DIAMINE

Mamedov, V. A.,Krokhina, L. V.,Il'yasov, A. V.

, p. 953 - 956 (2007/10/02)

It is established that the α-chloroepoxide methyl 2-chloro-3-(3-nitrophenyl)-2,3-epoxypropionate, in contrast to its α-chloroketone isomer methyl 3-(3-nitrophenyl)-3-chloro-2-oxopropionate, forms 2-(3-nitrophenyl)-3-methoxycarbonylquinoxaline in reaction

REACTION OF METHYL DICHLOROACETATE WITH SUBSTITUTED BENZALDEHYDES UNDER THE CONDITIONS OF THE DARZENS CONDENSATION

Mamedov, V. A.,Nuretdinov, I. A.

, p. 1690 - 1692 (2007/10/02)

We have found that condensation of methyl dichloroacetate (1) with benzaldehyde, p-chloro- and p-bromobenzaldehyde in t-BuOH in the presence of t-BuOK yields methyl 3-aryl-3-chloro-2-oxopropionates (3-5).In the case of nitrobenzaldehydes the reaction prod

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