Cas 90625-79-9,17-tert-Butyl-3,11-dithia-tricyclo[11.3.1.15,9]octadeca-1(16),5,7,9(18),13(17),14-hexaene

90625-79-9

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Product Name: 17-tert-Butyl-3,11-dithia-tricyclo[11.3.1.1^5,9]octadeca-1⁽¹⁶⁾,5,7,9⁽¹⁸⁾,13⁽¹⁷⁾,14-hexaene
Synonyms: 17-tert-Butyl-3,11-dithia-tricyclo[11.3.1.1^5,9]octadeca-1⁽¹⁶⁾,5,7,9⁽¹⁸⁾,13⁽¹⁷⁾,14-hexaene
CAS NO:90625-79-9
Molecular Formula:
Molecular Weight: 328.543
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: 17-tert-Butyl-3,11-dithia-tricyclo[11.3.1.1^5,9]octadeca-1⁽¹⁶⁾,5,7,9⁽¹⁸⁾,13⁽¹⁷⁾,14-hexaene(CAS DataBase Reference)
NIST Chemistry Reference: 17-tert-Butyl-3,11-dithia-tricyclo[11.3.1.1^5,9]octadeca-1⁽¹⁶⁾,5,7,9⁽¹⁸⁾,13⁽¹⁷⁾,14-hexaene(90625-79-9)
EPA Substance Registry System: 17-tert-Butyl-3,11-dithia-tricyclo[11.3.1.1^5,9]octadeca-1⁽¹⁶⁾,5,7,9⁽¹⁸⁾,13⁽¹⁷⁾,14-hexaene(90625-79-9)

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: 90625-79-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90625-79-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,2 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90625-79:
(7*9)+(6*0)+(5*6)+(4*2)+(3*5)+(2*7)+(1*9)=139
139 % 10 = 9
So 90625-79-9 is a valid CAS Registry Number.

90625-79-9Upstream product

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

90625-79-9Downstream Products

90625-79-9Relevant 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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