Cas 852945-55-2,((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ<sup>6</sup>-thia-4-aza-tricyclo[5.2.1.0<sup>1,5</sup>]dec-4-yl)-(2-phenyl-4,5-dihydro-oxazol-4-yl)-methanone

852945-55-2

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Product Name: ((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-(2-phenyl-4,5-dihydro-oxazol-4-yl)-methanone
Synonyms: ((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-(2-phenyl-4,5-dihydro-oxazol-4-yl)-methanone
CAS NO:852945-55-2
Molecular Formula:
Molecular Weight: 388.488
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: ((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-(2-phenyl-4,5-dihydro-oxazol-4-yl)-methanone(CAS DataBase Reference)
NIST Chemistry Reference: ((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-(2-phenyl-4,5-dihydro-oxazol-4-yl)-methanone(852945-55-2)
EPA Substance Registry System: ((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-(2-phenyl-4,5-dihydro-oxazol-4-yl)-methanone(852945-55-2)

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 852945-55-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 852945-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,9,4 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 852945-55:
(8*8)+(7*5)+(6*2)+(5*9)+(4*4)+(3*5)+(2*5)+(1*5)=202
202 % 10 = 2
So 852945-55-2 is a valid CAS Registry Number.

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852945-55-2Relevant academic research and scientific papers

Enantioselective synthetic method for α-alkylserine via phase-transfer catalytic alkylation of 2-phenyl-2-oxazoline-4- carbonylcamphorsultam

Lee, Jihye,Lee, Yeon-Im,Kang, Myoung Joo,Lee, Yeon-Ju,Jeong, Byeong-Seon,Lee, Jeong-Hee,Kim, Mi-Jeong,Choi, Ji-Yeon,Ku, Jin-Mo,Park, Hyeung-Geun,Jew, Sang-Sup

, p. 4158 - 4161 (2005)

An enantioselective synthetic method for α-alkylserines by the phase-transfer catalytic alkylation of 2-phenyl-2-oxazoline-4- carbonylcamphorsultam (4a) was developed. The phase-transfer catalytic a-alkylation of 4a using P2-Et at -78 °C gave α-alkylation

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