Cas 1201682-08-7,2-(cyclopropanecarbonyl)-6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline-1-carbaldehyde

1201682-08-7

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Basic information

Product Name: 2-(cyclopropanecarbonyl)-6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline-1-carbaldehyde
Synonyms: 2-(cyclopropanecarbonyl)-6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline-1-carbaldehyde
CAS NO:1201682-08-7
Molecular Formula:
Molecular Weight: 365.429
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: 2-(cyclopropanecarbonyl)-6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline-1-carbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 2-(cyclopropanecarbonyl)-6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline-1-carbaldehyde(1201682-08-7)
EPA Substance Registry System: 2-(cyclopropanecarbonyl)-6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline-1-carbaldehyde(1201682-08-7)

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: 1201682-08-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1201682-08-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,6,8 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1201682-08:
(9*1)+(8*2)+(7*0)+(6*1)+(5*6)+(4*8)+(3*2)+(2*0)+(1*8)=107
107 % 10 = 7
So 1201682-08-7 is a valid CAS Registry Number.

1201682-08-7Upstream product

1201682-01-0 cyclopropyl-(7,8-dimethoxy-1-phenyl-4,5-dihydro-1H-benzo[d]azepin-3(2H)-yl)methanone

1201682-08-7Downstream Products

1201682-14-5 (2-(cyclopropylmethyl)-6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinolin-1-yl)methanol

1201682-08-7Relevant academic research and scientific papers

FeCl3·6H2O-promoted skeleton-rearrangement of 1-substituted-3-benzazepines: Substrate extension and product utilization

Zhang, Jing,Wu, Kui,Wang, Meining,Jiang, Jianqin,Zhang, Ao

experimental part, p. 842 - 848 (2011/03/19)

FeCl3·6H2O-promoted skeleton-rearrangement of 1-substituted-3-benzazepines was further exploited. Both 1-aryl- and 1-alkyl- or 1-alkenyl-benzazepines underwent this reaction smoothly. The rearrangement products were used to prepare a

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