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87910-09-6

2-propyl-3-butoxy-4-(4-chlorophenylthio)butanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 87910-09-6 Structure

  • Basic information

    1. Product Name: 2-propyl-3-butoxy-4-(4-chlorophenylthio)butanal
    2. Synonyms: 2-propyl-3-butoxy-4-(4-chlorophenylthio)butanal
    3. CAS NO:87910-09-6
    4. Molecular Formula:
    5. Molecular Weight: 328.903
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87910-09-6.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: 2-propyl-3-butoxy-4-(4-chlorophenylthio)butanal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-propyl-3-butoxy-4-(4-chlorophenylthio)butanal(87910-09-6)
    11. EPA Substance Registry System: 2-propyl-3-butoxy-4-(4-chlorophenylthio)butanal(87910-09-6)

  • 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: 87910-09-6(Hazardous Substances Data)

87910-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87910-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,1 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87910-09:
(7*8)+(6*7)+(5*9)+(4*1)+(3*0)+(2*0)+(1*9)=156
156 % 10 = 6
So 87910-09-6 is a valid CAS Registry Number.

87910-09-6Downstream Products

87910-09-6Relevant articles and documents

A Novel Method of Crossed-Aldol Condensation: Alkylation of Trimethylsilyl Enol Ethers by Alkyl 1-Chloro-2-arylthioalkyl Ethers

Ibragimov, M. A.,Lazareva, M. I.,Smit, W. A.

, p. 880 - 884 (2007/10/02)

Trimethylsilyl enol ethers 5, derived from aldehydes or ketones, react with alkyl 1-chloro-2-arylthioalkyl ethers 3 (β-arylthio-α-chloroethers, prepared in situ from vinyl ethers 1 and arenesulfenyl chlorides 2) to give 2-alkoxy-3-arylthioalkyl ketone derivatives 6 in the presence of a Lewis acid.

REACTION OF SILYL ENOL ETHERS WITH β-HALOGENOALKYL ARYL SULFIDES - A METHOD OF β-ARYLTHIOALKYLATION OF CARBONYL COMPOUNDS

Ibragimov, M.A.,Smit, W.A.

, p. 961 - 964 (2007/10/02)

Reaction of β-halogenoalkyl aryl sulfides with silyl enol ethers in the presence of Lewis acids produced α-(β'-arylthioalkyl) substituted carbonyl compounds.

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