Cas 5173-11-5,6,13-dioxaheptacyclo[9.3.1.1~4,8~.0~2,10~.0~3,9~.0~5,7~.0~12,14~]hexadecane

5173-11-5

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Basic information

Product Name: 6,13-dioxaheptacyclo[9.3.1.1~4,8~.0~2,10~.0~3,9~.0~5,7~.0~12,14~]hexadecane
Synonyms:
CAS NO:5173-11-5
Molecular Formula: C₁₄H₁₆O₂
Molecular Weight: 216.2756
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 381.8°C at 760 mmHg
Flash Point: 160.2°C
Appearance: N/A
Density: 1.422g/cm³
Vapor Pressure: 1.08E-05mmHg at 25°C
Refractive Index: 1.659
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 6,13-dioxaheptacyclo[9.3.1.1~4,8~.0~2,10~.0~3,9~.0~5,7~.0~12,14~]hexadecane(CAS DataBase Reference)
NIST Chemistry Reference: 6,13-dioxaheptacyclo[9.3.1.1~4,8~.0~2,10~.0~3,9~.0~5,7~.0~12,14~]hexadecane(5173-11-5)
EPA Substance Registry System: 6,13-dioxaheptacyclo[9.3.1.1~4,8~.0~2,10~.0~3,9~.0~5,7~.0~12,14~]hexadecane(5173-11-5)

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: 5173-11-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 5173-11-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,7 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5173-11:
(6*5)+(5*1)+(4*7)+(3*3)+(2*1)+(1*1)=75
75 % 10 = 5
So 5173-11-5 is a valid CAS Registry Number.

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5173-11-5Downstream Products

5173-11-5Relevant academic research and scientific papers

Pd-catalyzed one-pot sequential unsymmetrical cross-coupling reactions of aryl/heteroaryl 1,2-dihalides

Danodia, Abhinandan K.,Saunthwal, Rakesh K.,Patel, Monika,Tiwari, Rakesh K.,Verma, Akhilesh K.

supporting information, p. 6487 - 6496 (2016/07/15)

Efficient, step-economic, Pd(ii)-catalyzed one-pot sequential Sonogashira/Sonogashira, Sonogashira/Suzuki, Sonogashira/Heck, Suzuki/Sonogashira, Suzuki/Suzuki, Suzuki/Heck, Heck/Sonogashira, Heck/Suzuki and Heck/Heck cross coupling reactions of sterically hindered aryl/heteroaryl 1,2-dihalides have been developed. The present methodology allows the conversion of easily available aryl/heteroaryl 1,2-dihalides into synthetically useful unsymmetrically substituted arenes/heteroarenes in good to excellent yields under mild reaction conditions. This methodology is a powerful tool for building a versatile substrate which can be utilized for the synthesis of various organic scaffolds.

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