Cas 114140-73-7,Methanone, phenyl[tetrahydro-4-[(methylnitrosoamino)oxy]-3-thienyl]-, S,S-dioxide

114140-73-7

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Basic information

Product Name: Methanone, phenyl[tetrahydro-4-[(methylnitrosoamino)oxy]-3-thienyl]-, S,S-dioxide
Synonyms:
CAS NO:114140-73-7
Molecular Formula: C12H14N2O5S
Molecular Weight: 298.32
EINECS: N/A
Product Categories: N/A
Mol File: 114140-73-7.mol

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: Methanone, phenyl[tetrahydro-4-[(methylnitrosoamino)oxy]-3-thienyl]-, S,S-dioxide(CAS DataBase Reference)
NIST Chemistry Reference: Methanone, phenyl[tetrahydro-4-[(methylnitrosoamino)oxy]-3-thienyl]-, S,S-dioxide(114140-73-7)
EPA Substance Registry System: Methanone, phenyl[tetrahydro-4-[(methylnitrosoamino)oxy]-3-thienyl]-, S,S-dioxide(114140-73-7)

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: 114140-73-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114140-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,4 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114140-73:
(8*1)+(7*1)+(6*4)+(5*1)+(4*4)+(3*0)+(2*7)+(1*3)=77
77 % 10 = 7
So 114140-73-7 is a valid CAS Registry Number.

114140-73-7Upstream product

114120-88-6 3-Phenyl-3a,4,6,6a-tetrahydro-thieno[3,4-d]isoxazole 5,5-dioxide

114140-73-7Downstream Products

114140-89-5 (4-Hydroxy-1,1-dioxo-tetrahydro-1λ⁶-thiophen-3-yl)-phenyl-methanone

114140-73-7Relevant academic research and scientific papers

A New, Efficient Approach to α,β-Unsaturated Ketones and β-Hydroxy Ketones From 4,5-Dihydroisoxazoles

Kwiatkowski, Stefan

, p. 1496 - 1498 (1987)

2-(N-Nitrosomethylamino-oxy)ethyl ketones (3), obtained from solvolysis with sodium nitrite of N-methyl-4,5-dihydroisoxazolium methylsulphates (2), were converted into α,β-unsaturated ketones (4) by treatment with base or into β-hydroxy ketones (5) by treatment with carboxylic acids.

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