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2-Mercapto-3-hydroxypropanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 15890-66-1 Structure
  • Basic information

    1. Product Name: 2-Mercapto-3-hydroxypropanal
    2. Synonyms: 2-Mercapto-3-hydroxypropanal;2-Thioglyceraldehyde;3-Hydroxy-2-mercaptopropanal;α-Mercaptoglyceraldehyde;alpha-Mercaptoglyceraldehyde;Glyceraldehyde, 2-mercapto-;Hydracrylaldehyde, 2-mercapto- (8ci);Propanal, 3-hydroxy-2-mercapto- (9ci)
    3. CAS NO:15890-66-1
    4. Molecular Formula: C3H6 O2 S
    5. Molecular Weight: 106.1435
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 15890-66-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 239.6°Cat760mmHg
    3. Flash Point: 98.7°C
    4. Appearance: /
    5. Density: 1.215g/cm3
    6. Vapor Pressure: 0.00698mmHg at 25°C
    7. Refractive Index: 1.496
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-Mercapto-3-hydroxypropanal(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Mercapto-3-hydroxypropanal(15890-66-1)
    12. EPA Substance Registry System: 2-Mercapto-3-hydroxypropanal(15890-66-1)
  • 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: 15890-66-1(Hazardous Substances Data)

15890-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15890-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,9 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15890-66:
(7*1)+(6*5)+(5*8)+(4*9)+(3*0)+(2*6)+(1*6)=131
131 % 10 = 1
So 15890-66-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H6O2S/c4-1-3(6)2-5/h1,3,5-6H,2H2

15890-66-1Upstream product

15890-66-1Downstream Products

15890-66-1Relevant articles and documents

Opening of thiiranes: Preparation of orthogonal protected 2-thioglyceraldehyde

Silvestri,Wong

, p. 910 - 914 (2007/10/03)

Treatment of acrolein diethyl acetal sulfide 8 with methanesulfenyl bromide at low temperature results in an efficient thiirane ring opening to a halo disulfide 9. The bromine in this halo disulfide is easily substituted by silver acetate, sodium azide, sodium iodide, and silver nitrate. Treatment of 9 with tetrabutylammonium acetate yields a novel dehydrohalogenation product 12. Silica gel converts bromide 9 into a disulfide-substituted version of acrolein 15. The orthogonal-protected version of 2-thioglyceraldehyde 13 can be deprotected to a useful form of this aldehyde.

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