Cas 1225287-50-2,ethyl 2-ethoxycarbonyl-4-methyl-5-(4-methylphenyl)methyl-5-hexenoate

1225287-50-2

Post Buying Request

Basic information

Product Name: ethyl 2-ethoxycarbonyl-4-methyl-5-(4-methylphenyl)methyl-5-hexenoate
Synonyms: ethyl 2-ethoxycarbonyl-4-methyl-5-(4-methylphenyl)methyl-5-hexenoate
CAS NO:1225287-50-2
Molecular Formula:
Molecular Weight: 332.44
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: ethyl 2-ethoxycarbonyl-4-methyl-5-(4-methylphenyl)methyl-5-hexenoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-ethoxycarbonyl-4-methyl-5-(4-methylphenyl)methyl-5-hexenoate(1225287-50-2)
EPA Substance Registry System: ethyl 2-ethoxycarbonyl-4-methyl-5-(4-methylphenyl)methyl-5-hexenoate(1225287-50-2)

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: 1225287-50-2(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1225287-50-2 Suppliers

Recommended suppliers

1225287-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1225287-50-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,5,2,8 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1225287-50:
(9*1)+(8*2)+(7*2)+(6*5)+(5*2)+(4*8)+(3*7)+(2*5)+(1*0)=142
142 % 10 = 2
So 1225287-50-2 is a valid CAS Registry Number.

1225287-50-2Upstream product

93638-77-8 3-methyl-4-methylene-cyclopentane-1,1-dicarboxylic acid diethyl ester

1225287-50-2Downstream Products

1225287-50-2Relevant academic research and scientific papers

Nickel-catalyzed arylative ring-opening of 3-methylenecycloalkane-1,1- dicarboxylates

Sumida, Yuto,Yorimitsu, Hideki,Oshima, Koichiro

supporting information; experimental part, p. 2254 - 2257 (2010/07/17)

An arylative ring-opening reaction of cyclic allylmalonates with arylzinc reagents under nickel catalysis has been developed. Upon the ring-opening sp3C-sp3C bond cleavage, the allylic moiety serves as an allylic electrophile to reac

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 1225287-50-2