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3878-55-5

3878-55-5

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3878-55-5 Usage

Chemical Properties

white crystalline powder

Uses

Mono-methyl Succinate is one of the substances used in the study of lactobacillus plantarum culture supernatants with potential pro-heating and anti-pathogenic properties in skin chronic wounds

Definition

ChEBI: A dicarboxylic acid monoester that is succinic acid in which one of the carboxy groups has been converted to its methyl ester.

Check Digit Verification of cas no

The CAS Registry Mumber 3878-55-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3878-55:
(6*3)+(5*8)+(4*7)+(3*8)+(2*5)+(1*5)=125
125 % 10 = 5
So 3878-55-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O4/c1-9-5(8)3-2-4(6)7/h2-3H2,1H3,(H,6,7)/p-1

3878-55-5 Well-known Company Product Price

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  • (Code)Product description
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  • Detail

  • Alfa Aesar

  • (H59722)  Methyl hydrogen succinate, 95%   

  • 3878-55-5

  • 25g

  • 636.0CNY

  • Detail

  • Alfa Aesar

  • (H59722)  Methyl hydrogen succinate, 95%   

  • 3878-55-5

  • 100g

  • 1778.0CNY

  • Detail

3878-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name monomethyl succinate

1.2 Other means of identification

Product number -
Other names mono-Methyl succinate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:3878-55-5 SDS

3878-55-5Relevant articles and documents

Synthesis of alaremycin

Wang, Yong-Gang,Wachi, Masaaki,Kobayashi, Yuichi

, p. 481 - 483 (2006)

Methyl 5-azido-4-oxohexanoate was synthesized from 5-hexenoic acid in six steps and converted to the title compound by NaReO4- and CF 3SO3H-catalyzed reaction in Ac2CVCCl4 followed by hydrolysis of the methyl ester moiety. Georg Thieme Verlag Stuttgart.

Complex Formation of Calcium Ions and Monosubstituted Succinic Acid Derivatives in Aqueous Solutions

Mitrofanova

, p. 17 - 19 (2003)

Complex formation of calcium ions with succinic acid monoamide and methyl hydrogen succinate at 25°C and ionic strength I = 0.3 (KC1) was studied by pH-potentiometric titration. The stability constants of the complexes were determined.

Inverse Electron-Demand Diels-Alder Bioconjugation Reactions Using 7-Oxanorbornenes as Dienophiles

Agramunt, Jordi,Ginesi, Rebecca,Grandas, Anna,Pedroso, Enrique

, p. 6593 - 6604 (2020/07/14)

Oligonucleotides, peptides, and peptide nucleic acids incorporating 7-oxanorbornene as a dienophile were reacted with tetrazines linked to either a peptide, d-biotin, BODIPY, or N-acetyl-d-galactosamine. The inverse electron-demand Diels-Alder (IEDDA) cycloaddition, which was performed overnight at 37 °C, in all cases furnished the target conjugate in good yields. IEDDA reactions with 7-oxanorbornenes produce a lower number of stereoisomers than that of IEDDA cycloadditions with other dienophiles.

Cyclohexyl-Fused, Spirobiindane-Derived, Phosphine-Catalyzed Synthesis of Tricyclic ?3-Lactams and Kinetic Resolution of ?3-Substituted Allenoates

Wu, Mingyue,Han, Zhaobin,Li, Kaizhi,Wu, Ji'En,Ding, Kuiling,Lu, Yixin

supporting information, p. 16362 - 16373 (2019/10/16)

A C2-symmetric chiral phosphine catalyst, NUSIOC-Phos, which can be easily derived from cyclohexyl-fused spirobiindane, was introduced. A highly enantioselective domino process involving pyrrolidine-2,3-diones and γ-substituted allenoates catalyzed by NUSIOC-Phos has been disclosed. Diastereospecific tricyclic γ-lactams containing five contiguous stereogenic centers were obtained in high yields and with nearly perfect enantioselectivities. A kinetic resolution process of racemic γ-substituted allenoates was developed for the generation of optically enriched chiral allenoates.

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