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95680-13-0

1,3-Dithiane, 2-(cyclohexylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 95680-13-0 Structure

  • Basic information

    1. Product Name: 1,3-Dithiane, 2-(cyclohexylmethylene)-
    2. Synonyms:
    3. CAS NO:95680-13-0
    4. Molecular Formula: C11H18S2
    5. Molecular Weight: 214.396
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95680-13-0.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: 1,3-Dithiane, 2-(cyclohexylmethylene)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Dithiane, 2-(cyclohexylmethylene)-(95680-13-0)
    11. EPA Substance Registry System: 1,3-Dithiane, 2-(cyclohexylmethylene)-(95680-13-0)

  • 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: 95680-13-0(Hazardous Substances Data)

95680-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95680-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,8 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 95680-13:
(7*9)+(6*5)+(5*6)+(4*8)+(3*0)+(2*1)+(1*3)=160
160 % 10 = 0
So 95680-13-0 is a valid CAS Registry Number.

95680-13-0Relevant articles and documents

Highly enantioselective oxidations of ketene dithioacetals leading to trans bis-sulfoxides

Aggarwal, Varinder K.,Steele, Rebecca M.,Ritmaleni,Barrell, Juliet K.,Grayson, Ian

, p. 4087 - 4090 (2003)

Ketene dithioacetals undergo a Sharpless-type asymmetric oxidation using (+)-DET, Ti(OZPr)4, and cumene hydroperoxide to give the trans bis-sulfoxides 4a-f with essentially complete control of enantioselectivity and dia-stereoselectivity. The high enantio

Trimethylsilyloxide-Catalysed Peterson Olefinations with 2,2-Bis(trimethylsilyl)-1,3-dithiane

Manvar, Atul,O'Shea, Donal F.

supporting information, p. 7259 - 7263 (2015/11/25)

The synthesis of the reagent 2,2-bis(trimethylsilyl)-1,3-dithiane was directly achieved in an excellent yield from 1,3-dithiane in one step. The bench-stable reagent can be utilized for Peterson olefinations using either TMSOK/Bu4NCl or fluorid

PREPARATION OF ALKENYL SULFIDES AND ENAMINES BY ALKYLIDENATION OF CARBOXYLIC ACID DERIVATIVES

Takai, Kazuhiko,Fujimura, Osamu,Kataoka, Yasutaka,Utimoto, Kiitiro

, p. 211 - 214 (2007/10/02)

Treatment of S-alkyl thioesters with a reagent prepared from RCHBr2, Zn, TiCl4, and TMEDA in THF at 25 degC gives Z-alkenyl sulfides selectively in good to excellent yields.Using the alkylidenation method, ketene dithioacetals and enamines are produced fr

DEALKYLATIVE DECARBOXYLATION.IV. A NOVEL APPROACH TO KETENE THIOACETALS

Belletire, J.L.,Walley, D.R.,Fremont,S.L.

, p. 5729 - 5732 (2007/10/02)

Reaction of 2-carbomethoxy-1,3-dithiane enolate with an equimolar mixture of trimethylacetyl chloride and an aldehyde followed by dealkylative decarboxylation of the resulting pivalate yields ketene thioacetals.

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