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CAS

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112701-05-0

α-(2-methyl-1,3-dithian-2-yl)benzylimine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 112701-05-0 Structure

  • Basic information

    1. Product Name: α-(2-methyl-1,3-dithian-2-yl)benzylimine
    2. Synonyms:
    3. CAS NO:112701-05-0
    4. Molecular Formula:
    5. Molecular Weight: 237.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112701-05-0.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: α-(2-methyl-1,3-dithian-2-yl)benzylimine(CAS DataBase Reference)
    10. NIST Chemistry Reference: α-(2-methyl-1,3-dithian-2-yl)benzylimine(112701-05-0)
    11. EPA Substance Registry System: α-(2-methyl-1,3-dithian-2-yl)benzylimine(112701-05-0)

  • 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: 112701-05-0(Hazardous Substances Data)

112701-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112701-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,0 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112701-05:
(8*1)+(7*1)+(6*2)+(5*7)+(4*0)+(3*1)+(2*0)+(1*5)=70
70 % 10 = 0
So 112701-05-0 is a valid CAS Registry Number.

112701-05-0Relevant articles and documents

REACTIONS OF METALLATED 1,3-DITHIANES WITH CARBOXYLIC ACID DERIVATIVES

Page, Philip C. Bulman,van Niel, Monique B.,Westwood, Donald

, p. 269 - 276 (2007/10/02)

2-Lithio-1,3-dithiane and 2-lithio-2-trimethylsilyl-1,3-dithiane react with nitriles to afford primary aminoketene dithioacetals in good yields; these compounds exhibit marked ambident nucleophilicity.Use of other carboxylic acid derivatives as electrophi

Chemistry of Aminoketene Dithioacetals: Preparation of Protected α-Amino Aldehydes and Ketones and Formation of Nitrogen Heterocycles

Page, Philip C. Bulman,Niel, Monique B. van,Westwood, Donald

, p. 775 - 776 (2007/10/02)

The ambient anion (2) derived from primary aminoketene dithioacetal (1, R = Ph) reacts with alkyl halides at the carbon atom to give remarkably stable imines which may be reduced to give protected α-amino ketones using borane in quantitative yield, and un

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