Cas 293307-81-0,[(R)-1-(4,5-Dimethoxy-2-vinyl-phenyl)-ethyl]-(4-methoxy-naphthalen-1-yl)-amine

293307-81-0

Post Buying Request

Basic information

Product Name: [(R)-1-(4,5-Dimethoxy-2-vinyl-phenyl)-ethyl]-(4-methoxy-naphthalen-1-yl)-amine
Synonyms: [(R)-1-(4,5-Dimethoxy-2-vinyl-phenyl)-ethyl]-(4-methoxy-naphthalen-1-yl)-amine
CAS NO:293307-81-0
Molecular Formula:
Molecular Weight: 363.456
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: [(R)-1-(4,5-Dimethoxy-2-vinyl-phenyl)-ethyl]-(4-methoxy-naphthalen-1-yl)-amine(CAS DataBase Reference)
NIST Chemistry Reference: [(R)-1-(4,5-Dimethoxy-2-vinyl-phenyl)-ethyl]-(4-methoxy-naphthalen-1-yl)-amine(293307-81-0)
EPA Substance Registry System: [(R)-1-(4,5-Dimethoxy-2-vinyl-phenyl)-ethyl]-(4-methoxy-naphthalen-1-yl)-amine(293307-81-0)

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: 293307-81-0(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

293307-81-0 Suppliers

Recommended suppliers

293307-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 293307-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,3,0 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 293307-81:
(8*2)+(7*9)+(6*3)+(5*3)+(4*0)+(3*7)+(2*8)+(1*1)=150
150 % 10 = 0
So 293307-81-0 is a valid CAS Registry Number.

293307-81-0Upstream product

293307-81-0Downstream Products

293307-82-1 2-{4,5-Dimethoxy-2-[(R)-1-(4-methoxy-naphthalen-1-ylamino)-ethyl]-phenyl}-ethanol

293307-81-0Relevant academic research and scientific papers

A facile and efficient asymmetric synthesis of (+)-salsolidine

Taniyama, Daisuke,Hasegawa, Masayoshi,Tomioka, Kiyoshi

, p. 5533 - 5536 (2007/10/03)

A three-key step methodology involving a highly selective asymmetric addition of an organolithium reagent to an N-naphthalenylimine, cyclization and oxidative removal of the N-naphthalenyl group provided a facile and efficient synthetic way to (+)-salsolidine. (C) 2000 Elsevier Science Ltd.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 293307-81-0