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Dimethyl 1-benzylpyrrolidine-3,4-dicarboxylate, also known as dimethyl-2-benzylpyrrolidine-3,4-dicarboxylate, is a synthetic compound belonging to the class of pyrrolidine derivatives. It possesses potential analgesic and anti-inflammatory properties and is often utilized in the research and development of new pharmaceutical drugs for pain relief and anti-inflammatory effects.

607362-87-8

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607362-87-8 Usage

Uses

Used in Pharmaceutical Research:
Dimethyl 1-benzylpyrrolidine-3,4-dicarboxylate is used as a research compound for the development of new pharmaceutical drugs. It is employed for its potential analgesic and anti-inflammatory properties, which are being investigated for their efficacy in pain relief and treatment of inflammation.
Used in Chronic Pain Treatment:
Dimethyl 1-benzylpyrrolidine-3,4-dicarboxylate is used as a potential treatment for chronic pain conditions. It has demonstrated analgesic effects in animal studies and is currently under investigation for its applicability in managing chronic pain in humans.

Check Digit Verification of cas no

The CAS Registry Mumber 607362-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,3,6 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 607362-87:
(8*6)+(7*0)+(6*7)+(5*3)+(4*6)+(3*2)+(2*8)+(1*7)=158
158 % 10 = 8
So 607362-87-8 is a valid CAS Registry Number.

607362-87-8Relevant articles and documents

AMINOQUINAZOLINE DERIVATIVES AND THEIR SALTS AND METHODS OF USE

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Paragraph 0443-0444, (2014/08/19)

The present invention relates to the field of medicine. Provided herein are aminoquinazoline derivatives, their salts and pharmaceutical formulations useful in modulating the protein tyrosine kinase activity, and in modulating inter- and/or intra-cellular signaling. Also provided herein are pharmaceutically acceptable compositions comprising the aminoquinazoline compounds and methods of using the compositions in the treatment of hyperproliferative disorders in mammals, especially humans.

2-PHENYL-5-HETEROCYCLYL-TETRAHYDRO-2H-PYRAN-3-AMINE COMPOUNDS FOR USE IN THE TREATMENT OF DIABETES AND ITS ASSOCIATED DISORDERS

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Page/Page column 27; 28, (2014/05/07)

The present invention relates to novel compounds of the general formula (I) their tautomeric forms, their enantiomers, their diastereoisomers, their pharmaceutically accepted salts, or pro-drugs thereof, which are useful for the treatment or prevention of diabetes mellitus (DM), obesity and other metabolic disorders. The invention also relates to process for the manufacture of said compounds, and pharmaceutical compositions containing them and their use.

AMINOQUINAZOLINE DERIVATIVES AND THEIR SALTS AND METHODS OF USE

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Paragraph 00290, (2013/06/05)

The present invention relates to the field of medicine. Provided herein are aminoquinazoline derivatives, their salts and pharmaceutical formulations useful in modulating the protein tyrosine kinase activity, and in modulating inter-and/or intra-cellular signaling. Also provided herein are pharmaceutically acceptable compositions comprising the aminoquinazoline compounds and methods of using the compositions in the treatment of hyperproliferative disorders in mammals, especially humans.

A New and Efficient Strategy for Non-stabilized Azomethine Ylide via Photoinduced Electron Transfer (PET) Initiated Sequential Double Desilylation

Pandey, Ganesh,Lakshmaiah, G.,Kumaraswamy, G.

, p. 1313 - 1314 (2007/10/02)

A practical approach for generating non-stabilized azomethine ylide by PTE initiation is generated.

PYRROLIDINE AND α-METHYLENE-γ-LACTAM FROM THE CYCLIZATION OF α -ALKYLAMINOETHYL)ACRYLATE: SYNTHESIS OF AZA-SARCOMYCINS

Tarnchompoo, Bonkoch,Thebtaranonth, Chachanat,Thebtaranonth, Yodhathai

, p. 6675 - 6678 (2007/10/02)

Diene 1 readily adds primary amines to give 2 which can cyclize either in a Michael addition fashion or via a displacement reaction to give, respectively, pyrrolidine 3 or methylene lactam 4 which further isomerizes to 5 under the employed reaction conditions.Compound 4 can be obtained as the sole product from the reaction of diene precursor 7 with amines followed by vacuum pyrolysis

A DEFINITE EVIDENCE ON THE AMBIVALENT AZOMETHINE YLIDE INTERMEDIATE IN TRIFLUOROACETIC ACID- AND FLUORIDE ANION-PROMOTED 1,3-CYCLOADDITIONS INVOLVING THE SILICON-CARBON BOND CLEAVAGE

Terao, Yoshiyasu,Kotaki, Hiromi,Imai, Nobuyuki,Achiwa, Kazuo

, p. 896 - 898 (2007/10/02)

Trifluoroacetic acid- and fluoride anion-promoted 1,3-cycloadditions of N-benzyl-N-(methoxymethyl)trimethylsilylmethylamine to dipolarophiles were found to proceed via the ambivalent azomethine ylide intermediates.KEYWORDS - azomethine ylide; 1,3-cycloaddition; ambivalence; N-benzyl-N-(methoxymethyl)trimethylsilylmethylamine; dipolarophile

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