Cas 337919-18-3,<i>N</i>-(8-hydroxymethyl-4-methoxy-5,6,7,8-tetrahydro-naphthalen-1-yl)-benzamide

337919-18-3

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Basic information

Product Name: N-(8-hydroxymethyl-4-methoxy-5,6,7,8-tetrahydro-naphthalen-1-yl)-benzamide
Synonyms:
CAS NO:337919-18-3
Molecular Formula:
Molecular Weight: 311.381
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-(8-hydroxymethyl-4-methoxy-5,6,7,8-tetrahydro-naphthalen-1-yl)-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(8-hydroxymethyl-4-methoxy-5,6,7,8-tetrahydro-naphthalen-1-yl)-benzamide(337919-18-3)
EPA Substance Registry System: N-(8-hydroxymethyl-4-methoxy-5,6,7,8-tetrahydro-naphthalen-1-yl)-benzamide(337919-18-3)

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: 337919-18-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 337919-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,7,9,1 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 337919-18:
(8*3)+(7*3)+(6*7)+(5*9)+(4*1)+(3*9)+(2*1)+(1*8)=173
173 % 10 = 3
So 337919-18-3 is a valid CAS Registry Number.

337919-18-3Upstream product

337919-17-2 N-[8-(tert-butyl-dimethyl-silanyloxymethyl)-4-methoxy-5,8-dihydro-naphthalen-1-yl]-benzamide

337919-18-3Downstream Products

337919-18-3Relevant academic research and scientific papers

The Diels-Alder reactions of quinone imine ketals: A synthesis of the ergot skeleton

Banfield,Kerr

, p. 436 - 438 (2001)

The high pressure (13 kbar) Diels-Alder reaction of N-benzoyl-p-benzoquinone-mono-imine dimethyl ketal with an appropriate diene yields, after treatment with anhydrous acid, a dihydronaphthanilide. Conversion to the tricyclic skeleton of the ergot alkaloids is effected via a series of simple transformations.

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