Cas 90614-69-0,15-tert-Butyl-tricyclo[9.3.1.14,8]hexadeca-1(14),4,6,8(16),11(15),12-hexaene

90614-69-0

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Basic information

Product Name: 15-tert-Butyl-tricyclo[9.3.1.1^4,8]hexadeca-1⁽¹⁴⁾,4,6,8⁽¹⁶⁾,11⁽¹⁵⁾,12-hexaene
Synonyms: 15-tert-Butyl-tricyclo[9.3.1.1^4,8]hexadeca-1⁽¹⁴⁾,4,6,8⁽¹⁶⁾,11⁽¹⁵⁾,12-hexaene
CAS NO:90614-69-0
Molecular Formula:
Molecular Weight: 264.411
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: 15-tert-Butyl-tricyclo[9.3.1.1^4,8]hexadeca-1⁽¹⁴⁾,4,6,8⁽¹⁶⁾,11⁽¹⁵⁾,12-hexaene(CAS DataBase Reference)
NIST Chemistry Reference: 15-tert-Butyl-tricyclo[9.3.1.1^4,8]hexadeca-1⁽¹⁴⁾,4,6,8⁽¹⁶⁾,11⁽¹⁵⁾,12-hexaene(90614-69-0)
EPA Substance Registry System: 15-tert-Butyl-tricyclo[9.3.1.1^4,8]hexadeca-1⁽¹⁴⁾,4,6,8⁽¹⁶⁾,11⁽¹⁵⁾,12-hexaene(90614-69-0)

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: 90614-69-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90614-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,1 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90614-69:
(7*9)+(6*0)+(5*6)+(4*1)+(3*4)+(2*6)+(1*9)=130
130 % 10 = 0
So 90614-69-0 is a valid CAS Registry Number.

90614-69-0Upstream product

1985-64-4 2,6-dimethyl-t-butylbenzene

90614-69-0Downstream Products

90614-69-0Relevant academic research and scientific papers

CYCLOPHANES WITH LARGE INTERNAL SUBSTITUENTS. THE SYNTHESIS AND CONFORMATIONAL BEHAVIOR OF 2,11-DITHIAMETACYCLOPHANES AND A METHACYCLOPHANE WITH tert-BUTYL SUBSTITUENTS.

Mitchell, Reginald H.,Weerawarna, Kumudini S.,Bushnell, Gordon W.

, p. 907 - 910 (2007/10/02)

The preparation, 1Hmr spectra and stereochemistry of 1E, 3E, 2F, 3F, and 2G are described.The stereochemistry of 3E is supported by an X-ray structure determination.

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