Cas 1350801-58-9,3-acetylamino-1,1-dioxo-2,3-dihydro-1H-1λ6-thiophene-3-carboxylic acid (-)-menthyl ester

1350801-58-9

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Basic information

Product Name: 3-acetylamino-1,1-dioxo-2,3-dihydro-1H-1λ6-thiophene-3-carboxylic acid (-)-menthyl ester
Synonyms: 3-acetylamino-1,1-dioxo-2,3-dihydro-1H-1λ6-thiophene-3-carboxylic acid (-)-menthyl ester
CAS NO:1350801-58-9
Molecular Formula:
Molecular Weight: 357.471
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: 3-acetylamino-1,1-dioxo-2,3-dihydro-1H-1λ6-thiophene-3-carboxylic acid (-)-menthyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-acetylamino-1,1-dioxo-2,3-dihydro-1H-1λ6-thiophene-3-carboxylic acid (-)-menthyl ester(1350801-58-9)
EPA Substance Registry System: 3-acetylamino-1,1-dioxo-2,3-dihydro-1H-1λ6-thiophene-3-carboxylic acid (-)-menthyl ester(1350801-58-9)

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: 1350801-58-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1350801-58-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,0,8,0 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1350801-58:
(9*1)+(8*3)+(7*5)+(6*0)+(5*8)+(4*0)+(3*1)+(2*5)+(1*8)=129
129 % 10 = 9
So 1350801-58-9 is a valid CAS Registry Number.

1350801-58-9Upstream product

1350801-57-8 4-acetoxy-3-acetylamino-1,1-dioxo-tetrahydro-1λ6-thiophene-3-carboxylic acid (-)-menthyl ester

1350801-58-9Downstream Products

1350801-58-9Relevant academic research and scientific papers

1,4-Dithiane-2,5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes

Baricordi, Nikla,Benetti, Simonetta,Bertolasi, Valerio,De Risi, Carmela,Pollini, Gian P.,Zamberlan, Francesco,Zanirato, Vinicio

, p. 208 - 213 (2012)

'One-pot' tandem reactions of commercially available 1,4-dithiane-2,5-diol (the dimer of mercaptoacetaldehyde) with electrophilic alkenes resulted in the facile formation of substituted tetrahydrothiophene derivatives. Thus, sulfa-Michael/Henry and sulfa-

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