Cas 906357-09-3,Benzoic acid (3aR,5S,6S,6aR)-2,2-dimethyl-6-(2,2,2-trichloro-acetylamino)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester

906357-09-3

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Basic information

Product Name: Benzoic acid (3aR,5S,6S,6aR)-2,2-dimethyl-6-(2,2,2-trichloro-acetylamino)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester
Synonyms: Benzoic acid (3aR,5S,6S,6aR)-2,2-dimethyl-6-(2,2,2-trichloro-acetylamino)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester
CAS NO:906357-09-3
Molecular Formula:
Molecular Weight: 464.73
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: Benzoic acid (3aR,5S,6S,6aR)-2,2-dimethyl-6-(2,2,2-trichloro-acetylamino)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (3aR,5S,6S,6aR)-2,2-dimethyl-6-(2,2,2-trichloro-acetylamino)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester(906357-09-3)
EPA Substance Registry System: Benzoic acid (3aR,5S,6S,6aR)-2,2-dimethyl-6-(2,2,2-trichloro-acetylamino)-6-vinyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester(906357-09-3)

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: 906357-09-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 906357-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,3,5 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 906357-09:
(8*9)+(7*0)+(6*6)+(5*3)+(4*5)+(3*7)+(2*0)+(1*9)=173
173 % 10 = 3
So 906357-09-3 is a valid CAS Registry Number.

906357-09-3Upstream product

906357-09-3Downstream Products

906357-09-3Relevant academic research and scientific papers

One-pot transformation of trichloroacetamide into readily deprotectable carbamates

Nishikawa, Toshio,Urabe, Daisuke,Tomita, Miho,Tsujimoto, Takashi,Iwabuchi, Tomoko,Isobe, Minoru

, p. 3263 - 3265 (2006)

A trichloroacetamide group was converted to an isocyanate, which was in situ captured by a variety of alcohols in the presence of CuCl and n-BuN 4Cl to afford the corresponding carbamates. The scope and limitation of this transformation are als

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