Cas 76373-17-6,[1,1']Binaphthalenyl-2,2'-dicarboxylic acid bis-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester

76373-17-6

Post Buying Request

Basic information

Product Name: [1,1']Binaphthalenyl-2,2'-dicarboxylic acid bis-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester
Synonyms:
CAS NO:76373-17-6
Molecular Formula:
Molecular Weight: 618.857
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: [1,1']Binaphthalenyl-2,2'-dicarboxylic acid bis-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: [1,1']Binaphthalenyl-2,2'-dicarboxylic acid bis-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester(76373-17-6)
EPA Substance Registry System: [1,1']Binaphthalenyl-2,2'-dicarboxylic acid bis-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester(76373-17-6)

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: 76373-17-6(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

76373-17-6 Suppliers

Recommended suppliers

76373-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76373-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,7 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76373-17:
(7*7)+(6*6)+(5*3)+(4*7)+(3*3)+(2*1)+(1*7)=146
146 % 10 = 6
So 76373-17-6 is a valid CAS Registry Number.

76373-17-6Upstream product

76373-17-6Downstream Products

76373-17-6Relevant academic research and scientific papers

PARTIAL ASYMMETRIC SYNTHESIS OF ATROPISOMERIC 1,1'-BINAPHTHYLS VIA THE ULLMANN COUPLING REACTION OF CHIRAL ALCOHOL ESTERS OF 1-BROMO-2-NAPHTHOIC ACID

Miyano, Sotaro,Tobita, Masayuki,Suzuki, Shoji,Nishikawa, Yukio,Hashimoto, Harukichi

, p. 1027 - 1030 (2007/10/02)

The Ullmann coupling of 1-bromo-2-naphthoates of C-chiral alcohols of R- and S-configuration induced axial dissymmetry of R- and S-chirality, respctively, in the newly formed 1,1'-bond of the binaphthyls; the optical yield amounted up to 13percent where the chiral alcohol was l-menthol.

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 76373-17-6