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113138-64-0

Benzene, [(cyclohexylmethoxymethyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113138-64-0 Structure

  • Basic information

    1. Product Name: Benzene, [(cyclohexylmethoxymethyl)thio]-
    2. Synonyms:
    3. CAS NO:113138-64-0
    4. Molecular Formula: C14H20OS
    5. Molecular Weight: 236.378
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113138-64-0.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: Benzene, [(cyclohexylmethoxymethyl)thio]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, [(cyclohexylmethoxymethyl)thio]-(113138-64-0)
    11. EPA Substance Registry System: Benzene, [(cyclohexylmethoxymethyl)thio]-(113138-64-0)

  • 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: 113138-64-0(Hazardous Substances Data)

113138-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113138-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,1,3 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113138-64:
(8*1)+(7*1)+(6*3)+(5*1)+(4*3)+(3*8)+(2*6)+(1*4)=90
90 % 10 = 0
So 113138-64-0 is a valid CAS Registry Number.

113138-64-0Relevant articles and documents

Direct and indirect electrochemical generation of alkoxycarbenium ion pools from thioacetals

Matsumoto, Kouichi,Ueoka, Koji,Suzuki, Shinkiti,Suga, Seiji,Yoshida, Jun-ichi

experimental part, p. 10901 - 10907 (2010/02/27)

Thioacetals were found to be effective precursors to generate and accumulate alkoxycarbenium ions based on direct and indirect cation pool methods. Alkoxycarbenium ions thus generated reacted with carbon nucleophiles such as allylsilanes and enol silyl et

Lithium bromide, a novel and highly effective catalyst for monothioacetalization of acetals under mild reaction conditions

Ono,Negoro,Sato

, p. 1581 - 1583 (2007/10/03)

Lithium bromide is efficient as a catalyst for the monothioacetalization of acetals under mild reaction conditions to provide products in excellent yields with high chemoselectivity.

ACTIVATION AND SYNTHETIC APPLICATIONS OF THIOSTANNANES. THIOALKOXYLATION OF ACETALS

Sato, Tsuneo,Otera, Junzo,Nozaki, Hitosi

, p. 1209 - 1218 (2007/10/02)

The Sn-S bonds in thiostannanes, BunSn(SPh)4-n, are activated towards acetals in the presence of BF3*OEt2.Acetals of various aldehydes and ketones are converted into the corresponding monothioacetals under mild conditions.Employment of α-enal acetals induces Michael addition to give synthetically useful γ-alkoxyally sulfides.

Organotin-Mediated Preparation of Monothioacetals

Sato, Tsuneo,Kobayashi, Takamitsu,Gojo, Tamehisa,Yoshida, Enji,Otera, Junzo,Nozaki, Hitosi

, p. 1661 - 1664 (2007/10/02)

Monothioacetals are obtained by treating the corresponding acetals with organotin thiophenoxides in the presence of BF3*OEt2.The reaction proceeds under mild conditions to provide the desired compounds with high selectivity.

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