Cas 94953-08-9,2H-1,3-Oxazin-2-one, tetrahydro-4-(iodomethyl)-6-methyl-3-[(4-methylphenyl)sulfonyl]-

94953-08-9

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Basic information

Product Name: 2H-1,3-Oxazin-2-one, tetrahydro-4-(iodomethyl)-6-methyl-3-[(4-methylphenyl)sulfonyl]-
Synonyms:
CAS NO:94953-08-9
Molecular Formula: C13H16INO4S
Molecular Weight: 409.245
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: 2H-1,3-Oxazin-2-one, tetrahydro-4-(iodomethyl)-6-methyl-3-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 2H-1,3-Oxazin-2-one, tetrahydro-4-(iodomethyl)-6-methyl-3-[(4-methylphenyl)sulfonyl]-(94953-08-9)
EPA Substance Registry System: 2H-1,3-Oxazin-2-one, tetrahydro-4-(iodomethyl)-6-methyl-3-[(4-methylphenyl)sulfonyl]-(94953-08-9)

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: 94953-08-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 94953-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,9,5 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94953-08:
(7*9)+(6*4)+(5*9)+(4*5)+(3*3)+(2*0)+(1*8)=169
169 % 10 = 9
So 94953-08-9 is a valid CAS Registry Number.

94953-08-9Upstream product

95601-95-9 C₁₃H₁₇NO₄S

94953-08-9Downstream Products

94953-08-9Relevant academic research and scientific papers

CARBAMATE MEDIATED FUNCTIONALIZATION OF UNSATURATED ALCOHOLS II. REGIO- AND STEREO-SELECTIVE SYNTHESIS OF 1,3-SYN AND 1,2-ANTI AMINO ALCOHOL DERIVATIVES VIA IODOCARBAMATION

Hirama, Masahiro,Iwashita, Mitsuko,Yamazaki, Yutaka,Ito, Sho

, p. 4963 - 4964 (2007/10/02)

A regio- and stereo-selective introduction of nitrogen functions to double bonds of acyclic, allylic and homoallylic alcohols was achieved via iodocyclization of the corresponding N-sulfonylated O-carbamates.

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