Cas 152593-90-3,(3S,4S,5S)-6-O-benzyl-4,5-O-isopropyliden-3,4,5,6-tetrahydroxy-1-(2-thiazolyl)-1-hexanone

152593-90-3

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Basic information

Product Name: (3S,4S,5S)-6-O-benzyl-4,5-O-isopropyliden-3,4,5,6-tetrahydroxy-1-(2-thiazolyl)-1-hexanone
Synonyms: (3S,4S,5S)-6-O-benzyl-4,5-O-isopropyliden-3,4,5,6-tetrahydroxy-1-(2-thiazolyl)-1-hexanone
CAS NO:152593-90-3
Molecular Formula:
Molecular Weight: 377.461
EINECS: N/A
Product Categories: N/A
Mol File: 152593-90-3.mol
Article Data: 1

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: (3S,4S,5S)-6-O-benzyl-4,5-O-isopropyliden-3,4,5,6-tetrahydroxy-1-(2-thiazolyl)-1-hexanone(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4S,5S)-6-O-benzyl-4,5-O-isopropyliden-3,4,5,6-tetrahydroxy-1-(2-thiazolyl)-1-hexanone(152593-90-3)
EPA Substance Registry System: (3S,4S,5S)-6-O-benzyl-4,5-O-isopropyliden-3,4,5,6-tetrahydroxy-1-(2-thiazolyl)-1-hexanone(152593-90-3)

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: 152593-90-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 152593-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,5,9 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 152593-90:
(8*1)+(7*5)+(6*2)+(5*5)+(4*9)+(3*3)+(2*9)+(1*0)=143
143 % 10 = 3
So 152593-90-3 is a valid CAS Registry Number.

152593-90-3Upstream product

152593-90-3Downstream Products

152593-90-3Relevant articles and documents

Iterative methodology for the stereocontrolled synthesis of polyol chains employing 2-acetylthiazole as lactaldehyde equivalent

Dondoni,Merino

, p. 903 - 908 (1993)

The anti-diastereoselective addition (ds 90-92%) of the lithium enolate of 2-acetylthiazole to chiral (poly)alkoxy aldehydes and the stereocontrolled ketone reduction of the resultant aldols using diisobutylaluminum hydride/tetramethylammonium triacetoxyb

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