Cas 127787-60-4,N-[2-Hydroxy-2-(4-methoxy-phenyl)-ethyl]-3,4-dimethoxy-N-methyl-benzamide

127787-60-4

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Basic information

Product Name: N-[2-Hydroxy-2-(4-methoxy-phenyl)-ethyl]-3,4-dimethoxy-N-methyl-benzamide
Synonyms: N-[2-Hydroxy-2-(4-methoxy-phenyl)-ethyl]-3,4-dimethoxy-N-methyl-benzamide
CAS NO:127787-60-4
Molecular Formula:
Molecular Weight: 345.395
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: N-[2-Hydroxy-2-(4-methoxy-phenyl)-ethyl]-3,4-dimethoxy-N-methyl-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[2-Hydroxy-2-(4-methoxy-phenyl)-ethyl]-3,4-dimethoxy-N-methyl-benzamide(127787-60-4)
EPA Substance Registry System: N-[2-Hydroxy-2-(4-methoxy-phenyl)-ethyl]-3,4-dimethoxy-N-methyl-benzamide(127787-60-4)

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: 127787-60-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127787-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,8 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127787-60:
(8*1)+(7*2)+(6*7)+(5*7)+(4*8)+(3*7)+(2*6)+(1*0)=164
164 % 10 = 4
So 127787-60-4 is a valid CAS Registry Number.

127787-60-4Upstream product

127787-60-4Downstream Products

23330-76-9 6,7-dimethoxy-4-(4-methoxyphenyl)-2-methyl-1, 2, 3, 4-tetrahydroisoquinoline

127787-60-4Relevant academic research and scientific papers

α'-SILYLATED TERTIARY BENZAMIDES AS DUAL ORTHO- AND α'-CARBANION SYNTHONS. CARBODESILYLATIVE ROUTES TO ISOQUINOLINE AND DIBENZOQUINOLIZIDINE DERIVATIVES

Cuevas, J.-C.,Snieckus, V.

, p. 5837 - 5840 (2007/10/02)

α'-Silylated benzamides 4a display both ortho (6)- and α'-carbanion (5h, 15) reactivities which are translated into new synthetic routes for isoquinoline (8, 18, 19) and protoberberine (11, 12) derivatives.

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