Cas 1375489-01-2,2(1,3)-benzena-1<sup>(4)</sup>,3<sup>(4)</sup>-diphenyl-4,8-dithia-6-thio-(1,3)(3,5)-1,2,4-triazolacyclooctaphan

1375489-01-2

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Basic information

Product Name: 2(1,3)-benzena-1⁽⁴⁾,3⁽⁴⁾-diphenyl-4,8-dithia-6-thio-(1,3)(3,5)-1,2,4-triazolacyclooctaphan
Synonyms:
CAS NO:1375489-01-2
Molecular Formula:
Molecular Weight: 498.656
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: 2(1,3)-benzena-1⁽⁴⁾,3⁽⁴⁾-diphenyl-4,8-dithia-6-thio-(1,3)(3,5)-1,2,4-triazolacyclooctaphan(CAS DataBase Reference)
NIST Chemistry Reference: 2(1,3)-benzena-1⁽⁴⁾,3⁽⁴⁾-diphenyl-4,8-dithia-6-thio-(1,3)(3,5)-1,2,4-triazolacyclooctaphan(1375489-01-2)
EPA Substance Registry System: 2(1,3)-benzena-1⁽⁴⁾,3⁽⁴⁾-diphenyl-4,8-dithia-6-thio-(1,3)(3,5)-1,2,4-triazolacyclooctaphan(1375489-01-2)

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Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1375489-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1375489-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,5,4,8 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1375489-01:
(9*1)+(8*3)+(7*7)+(6*5)+(5*4)+(4*8)+(3*9)+(2*0)+(1*1)=192
192 % 10 = 2
So 1375489-01-2 is a valid CAS Registry Number.

1375489-01-2Upstream product

1375488-98-4 2(1,3)-benzena-1⁽⁴⁾,3⁽⁴⁾-diphenyl-4,8-dithia-6-oxo-(1,3)(3,5)-1,2,4-triazolacyclooctaphane

1375489-01-2Downstream Products

1375489-01-2Relevant academic research and scientific papers

Novel synthesis of 1,2,4-triazolophanes and 1,3,4-oxadiazolophanes: A dieckmann condensation approach

Chande, Madhukar S.,Sajithkumar,Mondkar, Hemant S.,Barve, Pravin A.,Diwan, Sachin

scheme or table, p. 329 - 335 (2012/06/18)

The Dieckmann condensation has been used for the first time for the syntheses of novel 1,2,4-triazolophanes and 1,3,4-oxadiazolophanes. The bis-1,3,4-oxadiazol-2-thiols 1a and 1b were reacted with ethyl bromoacetate to give the diesters 2a and 2b. Diester

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