Cas 104846-38-0,1,4-cyclohexanedione mono-2,2-dimethyl trimethylene ketal 2,4,6-triisopropylphenyl sulfonyl hydrazone

104846-38-0

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Basic information

Product Name: 1,4-cyclohexanedione mono-2,2-dimethyl trimethylene ketal 2,4,6-triisopropylphenyl sulfonyl hydrazone
Synonyms:
CAS NO:104846-38-0
Molecular Formula:
Molecular Weight: 478.696
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: 1,4-cyclohexanedione mono-2,2-dimethyl trimethylene ketal 2,4,6-triisopropylphenyl sulfonyl hydrazone(CAS DataBase Reference)
NIST Chemistry Reference: 1,4-cyclohexanedione mono-2,2-dimethyl trimethylene ketal 2,4,6-triisopropylphenyl sulfonyl hydrazone(104846-38-0)
EPA Substance Registry System: 1,4-cyclohexanedione mono-2,2-dimethyl trimethylene ketal 2,4,6-triisopropylphenyl sulfonyl hydrazone(104846-38-0)

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: 104846-38-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104846-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,4 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104846-38:
(8*1)+(7*0)+(6*4)+(5*8)+(4*4)+(3*6)+(2*3)+(1*8)=120
120 % 10 = 0
So 104846-38-0 is a valid CAS Registry Number.

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104846-38-0Relevant academic research and scientific papers

Cycloadditions and annulations of transition metal carbene complexes

Wulff, William D.,Tang, Peng-Cho,Chan, Kin-Shing,McCallum, J.Stuart,Yang, Dominic C.,Gilbertson, Scott R.

, p. 5813 - 5832 (1985)

The synthetic aspects of several reactions from the multifaceted chemistry of Fischer carbene complexes are examined. Their benzannulation reactions with acetylenes are utilized in the synthesis of anthracyclinones via two approaches which differ by begin

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