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30364-57-9

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30364-57-9 Usage

Chemical structure

2,5-Pyrrolidinedione, 1-[(4-methoxybenzoyl)oxy]-

Classification

Thienodiazepine

Uses

Sedative, anxiolytic, and hypnotic for anxiety, insomnia, and panic attacks

Mechanism of action

Enhances the effects of GABA neurotransmitter

Popularity

Common in medical field and as a research chemical

Risks

Potential for abuse and addiction

Recommendation

Close monitoring and regulation to prevent harm

Check Digit Verification of cas no

The CAS Registry Mumber 30364-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,6 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30364-57:
(7*3)+(6*0)+(5*3)+(4*6)+(3*4)+(2*5)+(1*7)=89
89 % 10 = 9
So 30364-57-9 is a valid CAS Registry Number.

30364-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxybenzoic acid 2,5-dioxo-1-pyrrolidinyl ester

1.2 Other means of identification

Product number -
Other names p-methoxybenzoic acid N-hydroxysuccinimidyl 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:30364-57-9 SDS

30364-57-9Relevant articles and documents

Homogeneous hydrogenation of substituted (Z) - ene-1,2-dicarbamates with rh(i) phosphine complexes

Altman, Janina,Ben-Ishai, Dov,Berkovich, Evelina

, p. 2515 - 2520 (1993)

Homogeneous hydrogenation of substituted (Z)-ene-1,2-di-(-)-(1R, 3R, 4S)-methylcarbamate catalysed by rhodium complexes containing (+)-(2S,3S) or (-)-(2R,3R)-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane (DIOP) gives rise to the saturated

Formation of 1-hydroxymethylene-1,1-bisphosphinates through the addition of a silylated phosphonite on various trivalent derivatives

Dussart-Gautheret, Jade,Deschamp, Julia,Monteil, Maelle,Gager, Olivier,Legigan, Thibaut,Migianu-Griffoni, Evelyne,Lecouvey, Marc

, p. 14559 - 14569 (2020/12/29)

An easily handled one-pot synthetic procedure was previously developed for the synthesis of bisphosphinates starting from acyl chlorides. Herein, other trivalent derivatives as acid anhydrides and activated esters were tested to form various bisphosphinates. This modulation of the reactivity can be controlled according to the nature of the acid derivative for the use of sensitive and functionalized substrates.

Iron-Nitrate-Catalyzed Oxidative Esterification of Aldehydes and Alcohols with N-Hydroxyphthalimide: Efficient Synthesis of N-Hydroxyimide Esters

Xu, Xiaohe,Sun, Jian,Lin, Yuyan,Cheng, Jingya,Li, Pingping,Jiang, Xiaoying,Bai, Renren,Xie, Yuanyuan

supporting information, p. 7160 - 7166 (2017/12/28)

An Fe(NO3)3·9H2O-catalyzed cross-dehydrogenative coupling reaction between N-hydroxyphthalimide (NHPI) or N-hydroxysuccinimide (NHSI) and aldehydes or alcohols in air is described. This transformation represents an efficient approach to the preparation of N-hydroxyimide ester derivatives in moderate to excellent yields, and has a wide substrate scope.

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