Cas 1374301-55-9,(2S,3E)-1-[(3S)-4-benzyl-2-thioxothiazolidin-3-yl]-5-chloro-4-iodo-2-methylpent-3-en-1-one

1374301-55-9

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Basic information

Product Name: (2S,3E)-1-[(3S)-4-benzyl-2-thioxothiazolidin-3-yl]-5-chloro-4-iodo-2-methylpent-3-en-1-one
Synonyms: (2S,3E)-1-[(3S)-4-benzyl-2-thioxothiazolidin-3-yl]-5-chloro-4-iodo-2-methylpent-3-en-1-one
CAS NO:1374301-55-9
Molecular Formula:
Molecular Weight: 465.807
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: (2S,3E)-1-[(3S)-4-benzyl-2-thioxothiazolidin-3-yl]-5-chloro-4-iodo-2-methylpent-3-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3E)-1-[(3S)-4-benzyl-2-thioxothiazolidin-3-yl]-5-chloro-4-iodo-2-methylpent-3-en-1-one(1374301-55-9)
EPA Substance Registry System: (2S,3E)-1-[(3S)-4-benzyl-2-thioxothiazolidin-3-yl]-5-chloro-4-iodo-2-methylpent-3-en-1-one(1374301-55-9)

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: 1374301-55-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1374301-55-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,3,0 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1374301-55:
(9*1)+(8*3)+(7*7)+(6*4)+(5*3)+(4*0)+(3*1)+(2*5)+(1*5)=139
139 % 10 = 9
So 1374301-55-9 is a valid CAS Registry Number.

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1374301-55-9Relevant academic research and scientific papers

Towards allopumiliotoxins: A concise synthesis of the indolizidine core

Vijaykumar, Bodduri V. D.,Mallesham, Pitchakuntla,Chandrasekhar, Srivari

, p. 988 - 994 (2012)

The common bicyclic indolizidine core present in several allopumiliotoxins was synthesized by the sequential use of a Crimmins' aldol reaction, an SOCl2-mediated SNi displacement, and an intramolecular nucleophilic acyl substitution (INAS) as the key transformations. A concise synthesis of the indolizidine core of allopumiliotoxins is described by using an aldol reaction, an SNi displacement and an intramolecular nucleophilic acyl substitution as key steps. Copyright

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