Cas 2807-15-0,5-Cyclohexyl-penten-<sup>(4)</sup>-in-<sup>(2)</sup>

2807-15-0

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Basic information

Product Name: 5-Cyclohexyl-penten-⁽⁴⁾-in-⁽²⁾
Synonyms: 5-Cyclohexyl-penten-⁽⁴⁾-in-⁽²⁾
CAS NO:2807-15-0
Molecular Formula:
Molecular Weight: 148.248
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-Cyclohexyl-penten-⁽⁴⁾-in-⁽²⁾(CAS DataBase Reference)
NIST Chemistry Reference: 5-Cyclohexyl-penten-⁽⁴⁾-in-⁽²⁾(2807-15-0)
EPA Substance Registry System: 5-Cyclohexyl-penten-⁽⁴⁾-in-⁽²⁾(2807-15-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 2807-15-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 2807-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2807-15:
(6*2)+(5*8)+(4*0)+(3*7)+(2*1)+(1*5)=80
80 % 10 = 0
So 2807-15-0 is a valid CAS Registry Number.

2807-15-0Upstream product

2807-15-0Downstream Products

2807-16-1 5-Cyclohexyl-penten-⁽³⁾-in-⁽¹⁾

2807-15-0Relevant academic research and scientific papers

Pd-Senphos Catalyzed trans-Selective Cyanoboration of 1,3-Enynes

Li, Bo,Liu, Shih-Yuan,Zhang, Yuanzhe

, p. 15928 - 15932 (2020)

The first trans-selective cyanoboration reaction of an alkyne, specifically a 1,3-enyne, is described. The reported palladium-catalyzed cyanoboration of 1,3-enynes is site-, regio-, and diastereoselective, and is uniquely enabled by the 1,4-azaborine-based Senphos ligand structure. Tetra-substituted alkenyl nitriles are obtained providing useful boron-dienenitrile building blocks that can be further functionalized. The utility of our method has been demonstrated with the synthesis of Satigrel, an anti-platelet aggregating agent.

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