Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1311408-35-1

trans-methyl-2-(hex-1-en-1-yl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1311408-35-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1311408-35-1 Structure

  • Basic information

    1. Product Name: trans-methyl-2-(hex-1-en-1-yl)benzoate
    2. Synonyms: trans-methyl-2-(hex-1-en-1-yl)benzoate
    3. CAS NO:1311408-35-1
    4. Molecular Formula:
    5. Molecular Weight: 218.296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1311408-35-1.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: trans-methyl-2-(hex-1-en-1-yl)benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-methyl-2-(hex-1-en-1-yl)benzoate(1311408-35-1)
    11. EPA Substance Registry System: trans-methyl-2-(hex-1-en-1-yl)benzoate(1311408-35-1)

  • 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: 1311408-35-1(Hazardous Substances Data)

1311408-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1311408-35-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,1,4,0 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1311408-35:
(9*1)+(8*3)+(7*1)+(6*1)+(5*4)+(4*0)+(3*8)+(2*3)+(1*5)=101
101 % 10 = 1
So 1311408-35-1 is a valid CAS Registry Number.

1311408-35-1Downstream Products

1311408-35-1Relevant articles and documents

Ligand-free nickel-catalyzed semihydrogenation of alkynes with sodium borohydride: A highly efficient and selective process for: Cis -alkenes under ambient conditions

Wen, Xin,Shi, Xiaozhen,Qiao, Xianliang,Wu, Zhilei,Bai, Guoyi

, p. 5372 - 5375 (2017)

We report a low-cost and efficient catalytic system, involving in situ generated ligand-free Ni NPs, methanol and sodium borohydride, for the semihydrogenation of alkynes under ambient conditions. This catalytic system exhibits remarkably high activity, satisfactory cis-selectivity for internal alkynes, good stability and general applicability.

Microwave-assisted Suzuki-Miyaura cross-coupling of 2-alkyl and 2-alkenyl-benzo-1,3,2-diazaborolanes

Hadebe, Siphamandla W.,Sithebe, Siphamandla,Robinson, Ross S.

, p. 4277 - 4282 (2011/06/26)

Nitrogen-based boronate esters, such as 2-octyl-benzo-1,3,2-diazaborolane, 2-phenethyl-benzo-1,3,2-diazaborolane, and 2-{(1E)-hexenyl}-benzo-1,3,2- diazaborolane have been shown to be suitable coupling partners with arylhalides in microwave accelerated Suzuki cross-coupling reactions. Reaction yields of up to 89% were achieved. The use of a silicon group attached to the nitrogen atom, proved to enhance the reactivity of 2-octyl-benzo-1,3,2-diazaborolane.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1311408-35-1