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CAS

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155266-94-7

DIMETHYL 3-(2-CHLOROACETYL)-1,3-THIAZOLANE-2,4-DICARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 155266-94-7 Structure

  • Basic information

    1. Product Name: DIMETHYL 3-(2-CHLOROACETYL)-1,3-THIAZOLANE-2,4-DICARBOXYLATE
    2. Synonyms: DIMETHYL 3-(2-CHLOROACETYL)-1,3-THIAZOLANE-2,4-DICARBOXYLATE
    3. CAS NO:155266-94-7
    4. Molecular Formula: C9H12ClNO5S
    5. Molecular Weight: 281.71
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 155266-94-7.mol

  • Chemical Properties

    1. Melting Point: 126-128°C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: DIMETHYL 3-(2-CHLOROACETYL)-1,3-THIAZOLANE-2,4-DICARBOXYLATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: DIMETHYL 3-(2-CHLOROACETYL)-1,3-THIAZOLANE-2,4-DICARBOXYLATE(155266-94-7)
    11. EPA Substance Registry System: DIMETHYL 3-(2-CHLOROACETYL)-1,3-THIAZOLANE-2,4-DICARBOXYLATE(155266-94-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 155266-94-7(Hazardous Substances Data)

155266-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155266-94-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,2,6 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 155266-94:
(8*1)+(7*5)+(6*5)+(5*2)+(4*6)+(3*6)+(2*9)+(1*4)=147
147 % 10 = 7
So 155266-94-7 is a valid CAS Registry Number.

155266-94-7Relevant articles and documents

3-Aminoacetylthiazolidine-4-carboxylate Esters and their 1-Thia-4-azaspiro[4.5]decane-3-carboxylate Derivatives. Synthesis and Stereochemical Properties

Pellegrini,Refouvelet,Dachet,Rouland,Robert

, p. 1685 - 1691 (2007/10/03)

Dimethyl thiazolidine-2,4-dicarboxylate 2 and ethyl 1-thia-4-azaspiro[4.5]decane-3-carboxylates 3-5 were obtained as a diastereoisomeric mixture while their 3-aminoacetyl derivatives were isolated in only one isomeric form. These reactions of N-acylation were stereoselective, which can be explained by an interconversion of the diastereoisomers via a seco intermediate. The 1H nmr analysis of amides 6 and 11 exhibited the presence of both cis and irons amide bond conformations, whereas only one cis conformation was observed for spiro amides 8-10 and 13-15.

Thiazolidine-2,4-dicarboxylic acid and its esters: Synthesis, in solution behaviour and regioselective cyclocondesation

Refouvelet,Robert,Couquelet,Tronche

, p. 77 - 80 (2007/10/02)

Thiazolidine-2,4-dicarboxylic acid 2 was obtained as a diastereoisomeric mixture from the condensation of glyoxylic acid with L(-)R-cysteine Σ. In solution behaviour studies suggested that the reaction proceeded through an acid catalyzed epimerization mechanism. The methyl esterification of 2 was stereoselective, which can be explained by an interconversion of 2a via a ring seco intermediate. Condensation of the dimethyl ester 3 or the dissymmetric diester 4 with phenyl isocyanate gave rise to the same hydantoin 5. N-acylation of diesters 3 or 4 followed by the reaction with benzylamine was regioselective leading to bicyclic derivatives 3-10.

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