Cas 88320-15-4,(2R,3R)-3-(4-Chloro-phenyl)-3-hydroxy-2-methyl-1-phenothiazin-10-yl-propan-1-one

88320-15-4

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Basic information

Product Name: (2R,3R)-3-(4-Chloro-phenyl)-3-hydroxy-2-methyl-1-phenothiazin-10-yl-propan-1-one
Synonyms: (2R,3R)-3-(4-Chloro-phenyl)-3-hydroxy-2-methyl-1-phenothiazin-10-yl-propan-1-one
CAS NO:88320-15-4
Molecular Formula:
Molecular Weight: 395.909
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)-3-(4-Chloro-phenyl)-3-hydroxy-2-methyl-1-phenothiazin-10-yl-propan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-3-(4-Chloro-phenyl)-3-hydroxy-2-methyl-1-phenothiazin-10-yl-propan-1-one(88320-15-4)
EPA Substance Registry System: (2R,3R)-3-(4-Chloro-phenyl)-3-hydroxy-2-methyl-1-phenothiazin-10-yl-propan-1-one(88320-15-4)

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: 88320-15-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88320-15-4 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, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88320-15:
(7*8)+(6*8)+(5*3)+(4*2)+(3*0)+(2*1)+(1*5)=134
134 % 10 = 4
So 88320-15-4 is a valid CAS Registry Number.

88320-15-4Upstream product

88320-15-4Downstream Products

88320-15-4Relevant 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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