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2,5-Pyrrolidinedione, 3-amino-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122996-35-4

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122996-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122996-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,9,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122996-35:
(8*1)+(7*2)+(6*2)+(5*9)+(4*9)+(3*6)+(2*3)+(1*5)=144
144 % 10 = 4
So 122996-35-4 is a valid CAS Registry Number.

122996-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-3-aminopyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names 3-amino-1-benzylpyrrolidine-2,5-dione

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:122996-35-4 SDS

122996-35-4Relevant academic research and scientific papers

Discovery of an Orally Active Small-Molecule Tumor Necrosis Factor-α Inhibitor

Sun, Weiguang,Wu, Yanli,Zheng, Mengzhu,Yang, Yueying,Liu, Yang,Wu, Canrong,Zhou, Yirong,Zhang, Yonghui,Chen, Lixia,Li, Hua

supporting information, p. 8146 - 8156 (2020/09/21)

Tumor necrosis factor α (TNF-α) is an important therapeutic target for rheumatoid arthritis, inflammatory bowel disease, and septic hepatitis. In this study, structure-based virtual ligand screening combined with in vitro and in vivo assays were applied.

Compound with TNF-alpha inhibition activity and application thereof

-

Paragraph 0006, (2020/07/13)

The invention provides a compound shown in a formula I, wherein substituent groups are defined in the specification. The provided compound is an effective TNF-alpha inhibitor, which can be used to treat autoimmune diseases.

Methods for making optically active 3-aminopyrrolidine-2,5-dione derivative and optically active 3-aminopyrrolidine derivative

-

Example 3, (2008/06/13)

A method for making an optically active 3-aminopyrrolidine-2,5-dione derivative represented by the formula (3) includes cyclizing an optically active asparagine ester derivative represented by the formula (1) or (2) or an acid salt thereof. The optically active 3-aminopyrrolidine-2,5-dione derivative represented by the formula (3) may be reduced to form an optically active 3-aminopyrrolidine derivative represented by the formula (9). When, in the formula (9), R1 is an unsubstituted or substituted benzyl group, the compound may be hydrogenated to obtain the corresponding 1-unsubstituted compound in which R1 is hydrogen.

Process for preparing 3-amino-1-benzylpyrrolidines

-

, (2008/06/13)

A process for preparing a 3-amino-1-benzyl-pyrrolidine of the formula STR1 in which R1 and R2 each independently is H or alkyl, and Ph is phenyl, comprising reacting a 1-benzyl-Δ3 -pyrroline-2,5-dione of the formula STR2 in which R3 and R4 each independently is H or alkyl, with a nitrogen nucleophile of the formula in which R5 is H, benzyl, naphthylmethyl or phenyl-CHR6, and R6 is C1 -C6 -alkyl or phenyl, to give an optionally substituted 3-amino-1-benzylpyrrolidine-2,5-dione of the formula STR3 and, if R5 ≠H, the protecting group R5 is subsequently cleaved off to give a 3-amino-1-benzylpyrrolidine-2,5-dione of the formula STR4 and completely reducing the carbonyl groups to form the 3-amino-1-benzylpyrrolidine of the formula (I).

Synthesis and anticonvulsant activity of racemic 2-amino-N-substituted succinimide derivatives

Crider,Kolczynski,Miskell

, p. 192 - 195 (2007/10/02)

Several derivatives of (R,S)-2-amino-N-substituted succinimides were synthesized and evaluated in mice against seizures produced by electroshock and pentylenetetrazol. The most active compound against both electroshock- and pentylenetetrazol-induced seizu

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