Cas 123355-83-9,(1S,4R)-1-<(1R)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-<2-(3,4-dimethoxyphenyl)-1-ethyl>-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

123355-83-9

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Basic information

Product Name: (1S,4R)-1-<(1R)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-<2-(3,4-dimethoxyphenyl)-1-ethyl>-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one
Synonyms: (1S,4R)-1-<(1R)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-<2-(3,4-dimethoxyphenyl)-1-ethyl>-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one
CAS NO:123355-83-9
Molecular Formula:
Molecular Weight: 537.653
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,4R)-1-<(1R)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-<2-(3,4-dimethoxyphenyl)-1-ethyl>-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (1S,4R)-1-<(1R)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-<2-(3,4-dimethoxyphenyl)-1-ethyl>-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one(123355-83-9)
EPA Substance Registry System: (1S,4R)-1-<(1R)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-<2-(3,4-dimethoxyphenyl)-1-ethyl>-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one(123355-83-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 123355-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 123355-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,3,5 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 123355-83:
(8*1)+(7*2)+(6*3)+(5*3)+(4*5)+(3*5)+(2*8)+(1*3)=109
109 % 10 = 9
So 123355-83-9 is a valid CAS Registry Number.

123355-83-9Upstream product

123279-31-2 (1S,4R)-1-<1,2,3,4-Tetrahydro-6,7-dimethoxy-1-<2-(3,4-dimethoxyphenyl)-2-oxo-1-ethyl>-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one

123355-83-9Downstream Products

123355-83-9Relevant academic research and scientific papers

Asymetric Electrophilic α-Amidoalkylation, VII: Generation, Crystal Structure, and Trapping Reactions of a Chiral 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline Derived N-Acyliminium Ion

Wanner, Klaus Th.,Praschak, Ilona,Nagel, Ulrich

, p. 335 - 350 (2007/10/02)

The camphanic acid amide 4 has efficiently been oxidized with triphenylcarbenium tetrafluoroborate (3) to yield the chiral N-acyliminium ion 1.Trapping reactions of 1 with the silyl nucleophiles 7a-c and 10a-f proceeded with stereoselective bond formation

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