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  • 17570-08-0 Structure
  • Basic information

    1. Product Name: D-Thiaproline
    2. Synonyms:
    3. CAS NO:17570-08-0
    4. Molecular Formula: C5H8O2S
    5. Molecular Weight: 133.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17570-08-0.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: D-Thiaproline(CAS DataBase Reference)
    10. NIST Chemistry Reference: D-Thiaproline(17570-08-0)
    11. EPA Substance Registry System: D-Thiaproline(17570-08-0)
  • 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: 17570-08-0(Hazardous Substances Data)

17570-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17570-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,7 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17570-08:
(7*1)+(6*7)+(5*5)+(4*7)+(3*0)+(2*0)+(1*8)=110
110 % 10 = 0
So 17570-08-0 is a valid CAS Registry Number.

17570-08-0Downstream Products

17570-08-0Relevant articles and documents

Early Development Scale-Up of a Novel CXCR Antagonist: Focus on Racemic and Stereoselective Routes of a Key Intermediate

Tabet, Samuel,Rodeville, Nicolas,Mathieu, Arnaud,Raffin, Catherine,Millois-Barbuis, Corinne,Musicki, Branislav,Muller, Franck,Gerfaud, Thibaud,Boiteau, Jean-Guy,Cardinaud, Isabelle

, p. 2032 - 2044 (2017)

Efforts toward a convenient and scalable process for the synthesis of a novel CXCR antagonist 1 are described, with a specific focus on a chiral key intermediate. Two generations of a racemic route have been developed for short-term deliveries, and a ster

Process for the preparation of optically active carboxylic acids and amide intermediates

-

, (2008/06/13)

The present invention provides a process for the preparation of optically active carboxylic acids of the formula I* or II* STR1 in which X is an oxygen or sulfur atom and n is 1 or 2. The process comprises reacting a racemic carboxylic acid I or II or its derivatives with an optically active 2-amino-carboxylic acid ester to give the diastereomeric carboxylic acid amides, separating the diastereomers and, after cleavage of the amide bond, isolating the optically active carboxylic acids of the general formula I* or II*. The invention also provides certain novel optically active carboxylic acid amides and a tetrahydrothiopyran-2-carboxylic acid.

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