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(+/-)-(2,4-dichlorobutyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1388181-90-5 Structure
  • Basic information

    1. Product Name: (+/-)-(2,4-dichlorobutyl)benzene
    2. Synonyms: (+/-)-(2,4-dichlorobutyl)benzene
    3. CAS NO:1388181-90-5
    4. Molecular Formula:
    5. Molecular Weight: 203.111
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1388181-90-5.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: (+/-)-(2,4-dichlorobutyl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-(2,4-dichlorobutyl)benzene(1388181-90-5)
    11. EPA Substance Registry System: (+/-)-(2,4-dichlorobutyl)benzene(1388181-90-5)
  • 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: 1388181-90-5(Hazardous Substances Data)

1388181-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1388181-90-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,8,1,8 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1388181-90:
(9*1)+(8*3)+(7*8)+(6*8)+(5*1)+(4*8)+(3*1)+(2*9)+(1*0)=195
195 % 10 = 5
So 1388181-90-5 is a valid CAS Registry Number.

1388181-90-5Downstream Products

1388181-90-5Relevant articles and documents

Triphosgene-amine base promoted chlorination of unactivated aliphatic alcohols

Villalpando, Andres,Ayala, Caitlan E.,Watson, Christopher B.,Kartika, Rendy

, p. 3989 - 3996 (2013/06/04)

Unactivated α-branched primary and secondary aliphatic alcohols have been successfully transformed into their corresponding alkyl chlorides in high yields upon treatment with a mixture of triphosgene and pyridine in dichloromethane at reflux. These mild chlorination conditions are high yielding, stereospecific, and well tolerated by numerous sensitive functionalities. Furthermore, no nuisance waste products are generated in the course of the reactions.

Chlorination of aliphatic primary alcohols via triphosgene-triethylamine activation

Ayala, Caitlan E.,Villalpando, Andres,Nguyen, Alex L.,McCandless, Gregory T.,Kartika, Rendy

supporting information; experimental part, p. 3676 - 3679 (2012/09/08)

Activation of primary aliphatic alcohols with triphosgene and triethylamine mixtures afforded either alkyl chloride or diethylcarbamate products, and the switch in selectivity appeared to be driven by sterics. The reaction conditions to achieve this highly useful transformation were unexceptionally mild and readily tolerated by a wide range of sensitive functionalities.

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