Cas 1369936-89-9,(2R,3R)-1-adamantyl 5-(4-methoxyphenyl)-3-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-2-carboxylate

1369936-89-9

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Basic information

Product Name: (2R,3R)-1-adamantyl 5-(4-methoxyphenyl)-3-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-2-carboxylate
Synonyms:
CAS NO:1369936-89-9
Molecular Formula:
Molecular Weight: 421.46
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: (2R,3R)-1-adamantyl 5-(4-methoxyphenyl)-3-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-1-adamantyl 5-(4-methoxyphenyl)-3-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-2-carboxylate(1369936-89-9)
EPA Substance Registry System: (2R,3R)-1-adamantyl 5-(4-methoxyphenyl)-3-(trifluoromethyl)-3,4-dihydro-2H-pyrrole-2-carboxylate(1369936-89-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
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Hazardous Substances Data: 1369936-89-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1369936-89-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,9,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1369936-89:
(9*1)+(8*3)+(7*6)+(6*9)+(5*9)+(4*3)+(3*6)+(2*8)+(1*9)=229
229 % 10 = 9
So 1369936-89-9 is a valid CAS Registry Number.

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1369936-89-9Relevant academic research and scientific papers

Partially saturated fluorinated heterocycles: Diastereo- and enantioselective synthesis of β-trifluoromethyl-pyrroline carboxylates

Kawai, Hiroyuki,Sugita, Yutaka,Tokunaga, Etsuko,Sato, Hiroyasu,Shiro, Motoo,Shibata, Norio

, p. 3632 - 3634 (2012/05/20)

The first asymmetric synthesis of β-trifluoromethylated pyrroline carboxylates has been achieved by organocatalytic conjugated addition of adamantyl glycine imine to β-trifluoromethylated enones, followed by a deprotection/cyclization/dehydration sequence.

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