Cas 768370-20-3,(2-methyl-1,3-dioxo-2,3,3a,4,10,10a-hexahydro-1<i>H</i>-9-thia-2-aza-cyclopenta[<i>b</i>]fluoren-4-yl)-carbamic acid benzyl ester

768370-20-3

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Product Name: (2-methyl-1,3-dioxo-2,3,3a,4,10,10a-hexahydro-1H-9-thia-2-aza-cyclopenta[b]fluoren-4-yl)-carbamic acid benzyl ester
Synonyms:
CAS NO:768370-20-3
Molecular Formula:
Molecular Weight: 420.489
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-methyl-1,3-dioxo-2,3,3a,4,10,10a-hexahydro-1H-9-thia-2-aza-cyclopenta[b]fluoren-4-yl)-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2-methyl-1,3-dioxo-2,3,3a,4,10,10a-hexahydro-1H-9-thia-2-aza-cyclopenta[b]fluoren-4-yl)-carbamic acid benzyl ester(768370-20-3)
EPA Substance Registry System: (2-methyl-1,3-dioxo-2,3,3a,4,10,10a-hexahydro-1H-9-thia-2-aza-cyclopenta[b]fluoren-4-yl)-carbamic acid benzyl ester(768370-20-3)

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 768370-20-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 768370-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,8,3,7 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 768370-20:
(8*7)+(7*6)+(6*8)+(5*3)+(4*7)+(3*0)+(2*2)+(1*0)=193
193 % 10 = 3
So 768370-20-3 is a valid CAS Registry Number.

768370-20-3Upstream product

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768370-20-3Relevant academic research and scientific papers

A new efficient synthesis of substituted luminols using multicomponent reactions

Neumann, Helfried,Klaus, Stefan,Klawonn, Markus,Strübing, Dirk,Hübner, Sandra,G?rdes, Dirk,Von Wangelin, Axel Jacobi,Lalk, Michael,Beller, Matthias

, p. 431 - 438 (2007/10/03)

A new general synthesis of substituted luminols (5-amino-2,3- dihydrophthalazine-1,4-diones) is presented. Diversely substituted luminol derivatives can be synthesized in three steps. The products are of interest as new materials, which exhibit chemiluminescence.

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