Cas 88320-03-0,(2R,3R)-1-(2,3-Dihydro-benzo[1,4]thiazin-4-yl)-3-hydroxy-2-methyl-3-phenyl-propan-1-one

88320-03-0

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Basic information

Product Name: (2R,3R)-1-(2,3-Dihydro-benzo[1,4]thiazin-4-yl)-3-hydroxy-2-methyl-3-phenyl-propan-1-one
Synonyms: (2R,3R)-1-(2,3-Dihydro-benzo[1,4]thiazin-4-yl)-3-hydroxy-2-methyl-3-phenyl-propan-1-one
CAS NO:88320-03-0
Molecular Formula:
Molecular Weight: 313.42
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: (2R,3R)-1-(2,3-Dihydro-benzo[1,4]thiazin-4-yl)-3-hydroxy-2-methyl-3-phenyl-propan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-1-(2,3-Dihydro-benzo[1,4]thiazin-4-yl)-3-hydroxy-2-methyl-3-phenyl-propan-1-one(88320-03-0)
EPA Substance Registry System: (2R,3R)-1-(2,3-Dihydro-benzo[1,4]thiazin-4-yl)-3-hydroxy-2-methyl-3-phenyl-propan-1-one(88320-03-0)

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: 88320-03-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88320-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,2 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88320-03:
(7*8)+(6*8)+(5*3)+(4*2)+(3*0)+(2*0)+(1*3)=130
130 % 10 = 0
So 88320-03-0 is a valid CAS Registry Number.

88320-03-0Upstream product

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88320-03-0Relevant academic research and scientific papers

ACYCLIC STEREOSELECTION. ERYTHROSELECTIVE ALDOL CONDENSATION OF 4-ACYL-2,3-DIHYDRO-4H-1,4-BENZOTHIAZINE AND 10-ACYLPHENOTHIAZINE.

Babudri, F.,Di Nunno, L.,Florio, S.

, p. 3883 - 3886 (2007/10/02)

The title amides undergo aldol-type cross-condensation providing aldols of exclusive erythro configuration.The preferred cis geometry of the precursor amide enolate is likely to be at origin of the erythro selection.

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