Cas 1379657-82-5,diethyl 2-(3-methoxyphenyl)-1,2,3,4-tetrahydroisoquinoline-1-yl-phosphonate

1379657-82-5

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Basic information

Product Name: diethyl 2-(3-methoxyphenyl)-1,2,3,4-tetrahydroisoquinoline-1-yl-phosphonate
Synonyms:
CAS NO:1379657-82-5
Molecular Formula:
Molecular Weight: 375.404
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: diethyl 2-(3-methoxyphenyl)-1,2,3,4-tetrahydroisoquinoline-1-yl-phosphonate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl 2-(3-methoxyphenyl)-1,2,3,4-tetrahydroisoquinoline-1-yl-phosphonate(1379657-82-5)
EPA Substance Registry System: diethyl 2-(3-methoxyphenyl)-1,2,3,4-tetrahydroisoquinoline-1-yl-phosphonate(1379657-82-5)

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: 1379657-82-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1379657-82-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,6,5 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1379657-82:
(9*1)+(8*3)+(7*7)+(6*9)+(5*6)+(4*5)+(3*7)+(2*8)+(1*2)=225
225 % 10 = 5
So 1379657-82-5 is a valid CAS Registry Number.

1379657-82-5Upstream product

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1379657-82-5Relevant academic research and scientific papers

Electrochemical Cross-Dehydrogenative Coupling of N-Aryl-tetrahydroisoquinolines with Phosphites and Indole

Xie, Wenxia,Liu, Nian,Gong, Bowen,Ning, Shulin,Che, Xin,Cui, Lili,Xiang, Jinbao

, p. 2498 - 2501 (2019)

A metal- and reagent-free, electrochemical cross-dehydrogenative coupling reaction of N-aryl-tetrahydroisoquinolines with phosphites and indole is developed. This method provides an environmentally benign and simple approach for the construction of C–P an

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