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  • 1016668-37-3 Structure
  • Basic information

    1. Product Name: C12H12
    2. Synonyms: C12H12
    3. CAS NO:1016668-37-3
    4. Molecular Formula:
    5. Molecular Weight: 156.227
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1016668-37-3.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: C12H12(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H12(1016668-37-3)
    11. EPA Substance Registry System: C12H12(1016668-37-3)
  • 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: 1016668-37-3(Hazardous Substances Data)

1016668-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1016668-37-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,6,6,6 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1016668-37:
(9*1)+(8*0)+(7*1)+(6*6)+(5*6)+(4*6)+(3*8)+(2*3)+(1*7)=143
143 % 10 = 3
So 1016668-37-3 is a valid CAS Registry Number.

1016668-37-3Downstream Products

1016668-37-3Relevant articles and documents

Stereo- And Regioselective cis-Hydrophosphorylation of 1,3-Enynes Enabled by the Visible-Light Irradiation of NiCl2(PPh3)2

Hou, Hong,Zhou, Bing,Wang, Jiawei,Zhao, Dengyang,Sun, Duhao,Chen, Xiaoyun,Han, Ying,Yan, Chaoguo,Shi, Yaocheng,Zhu, Shaoqun

, p. 2981 - 2987 (2021)

Described herein is a stereo- and regioselective cis-hydrophosphorylation reaction of the internal alkyne of 1,3-enynes that accesses various 1,3-dienes in good isolated yields. The visible-light irradiation of NiCl2(PPh3)2 allows the generation of highly reactive nickel(II)-phosphorus species that subsequently migrate into the internal alkyne of the 1,3-enynes and protonate the resulting vinyl nickel species, leading to various phosphinoyl 1,3-butadienes under mild reaction conditions.

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