Cas 1422347-05-4,(S,4Z,7E)-1-((S)-4-benzyl-2-thioxothiazolidin-3-yl)-3-hydroxy-5-methylnona-4,7-dien-1-one

1422347-05-4

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Basic information

Product Name: (S,4Z,7E)-1-((S)-4-benzyl-2-thioxothiazolidin-3-yl)-3-hydroxy-5-methylnona-4,7-dien-1-one
Synonyms: (S,4Z,7E)-1-((S)-4-benzyl-2-thioxothiazolidin-3-yl)-3-hydroxy-5-methylnona-4,7-dien-1-one
CAS NO:1422347-05-4
Molecular Formula:
Molecular Weight: 375.556
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: (S,4Z,7E)-1-((S)-4-benzyl-2-thioxothiazolidin-3-yl)-3-hydroxy-5-methylnona-4,7-dien-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (S,4Z,7E)-1-((S)-4-benzyl-2-thioxothiazolidin-3-yl)-3-hydroxy-5-methylnona-4,7-dien-1-one(1422347-05-4)
EPA Substance Registry System: (S,4Z,7E)-1-((S)-4-benzyl-2-thioxothiazolidin-3-yl)-3-hydroxy-5-methylnona-4,7-dien-1-one(1422347-05-4)

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: 1422347-05-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1422347-05-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,2,3,4 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1422347-05:
(9*1)+(8*4)+(7*2)+(6*2)+(5*3)+(4*4)+(3*7)+(2*0)+(1*5)=124
124 % 10 = 4
So 1422347-05-4 is a valid CAS Registry Number.

1422347-05-4Upstream product

1422347-03-2 (2Z,5E)-3-methylhepta-2,5-dienal

1422347-05-4Downstream Products

1422347-05-4Relevant academic research and scientific papers

Enantioselective synthesis of the C5-C23 segment of biselyngbyaside

Chandrasekhar, Srivari,Rajesh, Gontla,Naresh, Tumma

supporting information, p. 252 - 255 (2013/02/23)

Stereo and enantioselective synthesis of C5-C23 fragment of cytotoxic marine natural product biselyngbyaside is achieved using E-selective methyl lithium addition onto enyne, Crimmin's acetate aldol reaction, Sharpless asymmetric epoxidation, and Julia-Kocienski olefination as the key steps.

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