Cas 221099-74-7,(R)-Hydroxy-phenyl-acetic acid (1S,2R,4R)-1-(hydroxy-diphenyl-methyl)-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester

221099-74-7

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Basic information

Product Name: (R)-Hydroxy-phenyl-acetic acid (1S,2R,4R)-1-(hydroxy-diphenyl-methyl)-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester
Synonyms: (R)-Hydroxy-phenyl-acetic acid (1S,2R,4R)-1-(hydroxy-diphenyl-methyl)-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester
CAS NO:221099-74-7
Molecular Formula:
Molecular Weight: 456.582
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: (R)-Hydroxy-phenyl-acetic acid (1S,2R,4R)-1-(hydroxy-diphenyl-methyl)-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-Hydroxy-phenyl-acetic acid (1S,2R,4R)-1-(hydroxy-diphenyl-methyl)-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester(221099-74-7)
EPA Substance Registry System: (R)-Hydroxy-phenyl-acetic acid (1S,2R,4R)-1-(hydroxy-diphenyl-methyl)-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester(221099-74-7)

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: 221099-74-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 221099-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,0,9 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 221099-74:
(8*2)+(7*2)+(6*1)+(5*0)+(4*9)+(3*9)+(2*7)+(1*4)=117
117 % 10 = 7
So 221099-74-7 is a valid CAS Registry Number.

221099-74-7Upstream product

221099-74-7Downstream Products

221099-71-4 exo-10,10-diphenyl-10-hydroxymethyl-7,7-dimethylbicyclo[2.2.1]heptane-2-ol

221099-74-7Relevant academic research and scientific papers

Exo-10,10-diphenyl-2,10-camphanediol as a new chiral auxiliary in asymmetric reduction

Chen,Chu,Liao,Tsai,Wang,Chen

, p. 1141 - 1144 (1999)

Stereoselective reduction of α-keto ester derived from exo-10,10- diphenyl-2,10-camphanediol with various hydrides proceeded with high diastereoselectivities (≥ 96% de) to afford the corresponding α-hydroxy ester with excellent yields. Change of reducing

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