Cas 344957-26-2,18-tert-Butyl-17-methyl-3,11-dithia-tricyclo[11.3.1.15,9]octadeca-1(16),5,7,9(18),13(17),14-hexaene

344957-26-2

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Product Name: 18-tert-Butyl-17-methyl-3,11-dithia-tricyclo[11.3.1.1^5,9]octadeca-1⁽¹⁶⁾,5,7,9⁽¹⁸⁾,13⁽¹⁷⁾,14-hexaene
Synonyms:
CAS NO:344957-26-2
Molecular Formula:
Molecular Weight: 342.569
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: 18-tert-Butyl-17-methyl-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: 18-tert-Butyl-17-methyl-3,11-dithia-tricyclo[11.3.1.1^5,9]octadeca-1⁽¹⁶⁾,5,7,9⁽¹⁸⁾,13⁽¹⁷⁾,14-hexaene(344957-26-2)
EPA Substance Registry System: 18-tert-Butyl-17-methyl-3,11-dithia-tricyclo[11.3.1.1^5,9]octadeca-1⁽¹⁶⁾,5,7,9⁽¹⁸⁾,13⁽¹⁷⁾,14-hexaene(344957-26-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 344957-26-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 344957-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,9,5 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 344957-26:
(8*3)+(7*4)+(6*4)+(5*9)+(4*5)+(3*7)+(2*2)+(1*6)=172
172 % 10 = 2
So 344957-26-2 is a valid CAS Registry Number.

344957-26-2Upstream product

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

344957-26-2Downstream Products

344957-26-2Relevant 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 (1984)

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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