Cas 85809-60-5,Acetic acid (S)-(4-chloro-phenyl)-((S)-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-methyl ester

85809-60-5

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Basic information

Product Name: Acetic acid (S)-(4-chloro-phenyl)-((S)-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-methyl ester
Synonyms:
CAS NO:85809-60-5
Molecular Formula:
Molecular Weight: 361.849
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: Acetic acid (S)-(4-chloro-phenyl)-((S)-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (S)-(4-chloro-phenyl)-((S)-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-methyl ester(85809-60-5)
EPA Substance Registry System: Acetic acid (S)-(4-chloro-phenyl)-((S)-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-methyl ester(85809-60-5)

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: 85809-60-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85809-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,0 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85809-60:
(7*8)+(6*5)+(5*8)+(4*0)+(3*9)+(2*6)+(1*0)=165
165 % 10 = 5
So 85809-60-5 is a valid CAS Registry Number.

85809-60-5Upstream product

85809-60-5Downstream Products

85809-67-2 (Z)-2-(4-chlorobenzylidene)-4-methyl-2H-benzo[b][1,4]thiazin-3(4H)-one

85809-60-5Relevant academic research and scientific papers

STEREOSELECTIVE SYNTHESIS OF 2-ALKYLIDENE-3,4-DIHYDRO-3-OXO-2H-1,4-BENZOTHIAZINES

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

, p. 3059 - 3065 (2007/10/02)

Metallation of 4-methyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazine with LDA and subsequent reaction with aldehydes leads to diastereomeric aldols 4 and 5.Acetylation followed by acetic acid elimination of the aldols provides a stereoselective and high yield route to 2-alkylidene-3,4-dihydro-3-oxo-2H-1,4-benzothiazines.

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