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113366-60-2

5-Thiazolecarboxylic acid, 4-(3-hydroxypentyl)-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113366-60-2 Structure

  • Basic information

    1. Product Name: 5-Thiazolecarboxylic acid, 4-(3-hydroxypentyl)-2-phenyl-
    2. Synonyms:
    3. CAS NO:113366-60-2
    4. Molecular Formula: C15H17NO3S
    5. Molecular Weight: 291.371
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113366-60-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-Thiazolecarboxylic acid, 4-(3-hydroxypentyl)-2-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Thiazolecarboxylic acid, 4-(3-hydroxypentyl)-2-phenyl-(113366-60-2)
    11. EPA Substance Registry System: 5-Thiazolecarboxylic acid, 4-(3-hydroxypentyl)-2-phenyl-(113366-60-2)

  • 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: 113366-60-2(Hazardous Substances Data)

113366-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113366-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,6 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113366-60:
(8*1)+(7*1)+(6*3)+(5*3)+(4*6)+(3*6)+(2*6)+(1*0)=102
102 % 10 = 2
So 113366-60-2 is a valid CAS Registry Number.

113366-60-2Downstream Products

113366-60-2Relevant articles and documents

Regioselectivity in the Lithiation of Methyl-substituted Thiazole- and Oxazole-Carboxylic Acids and Carboxamides: General Methods for the Elaboration of Trisubstituted Thiazoles and Oxazoles

Cornwall, Philip,Dell, Colin P.,Knight, David W.

, p. 2417 - 2428 (2007/10/02)

A number of anionic intermediates have been developed which are suitable for the elaboration of trisubstituted thiazoles and oxazoles.Thus, deprotonation of 2,4-dimethylthiazole-5-carboxylic acid 9 using either BuLi or LDA occurs regiospecifically at the

NEW METHODS FOR THE HOMOLOGATION OF THIAZOLES AND OXAZOLES BY REGIOSPECIFIC LITHIATIONS OF THIAZOLE- AND OXAZOLE-CARBOXYLIC ACID DERIVATIVES.

Cornwall, Philip,Dell, Colin P.,Knight, David W.

, p. 3585 - 3588 (2007/10/02)

Dianions are obtained by regiospecific lithiations of the parent thiazole- and oxazole-carboxylic acids; when the 2-position is blocked by a phenyl group, 4-(or 5-) methyl groups can be lithiated in thiazole- or oxazole-5(or 4-)carboxylic acids .Lithiations of the 2,5-dimethyl isomers are not regiospecific while those of the corresponding N,N-diethylamides give exclusively the monoanions (14) and (17); all of these new intermediates react efficiently with a range of electrophiles.

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