Cas 342909-14-2,dimethyl (1'E,3'S)-2-(3'-acetoxy-4'-t-butyldiphenylsilyloxy-but-1'-enyl)-2-benzylmalonate

342909-14-2

Post Buying Request

Basic information

Product Name: dimethyl (1'E,3'S)-2-(3'-acetoxy-4'-t-butyldiphenylsilyloxy-but-1'-enyl)-2-benzylmalonate
Synonyms: dimethyl (1'E,3'S)-2-(3'-acetoxy-4'-t-butyldiphenylsilyloxy-but-1'-enyl)-2-benzylmalonate
CAS NO:342909-14-2
Molecular Formula:
Molecular Weight: 588.773
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: dimethyl (1'E,3'S)-2-(3'-acetoxy-4'-t-butyldiphenylsilyloxy-but-1'-enyl)-2-benzylmalonate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl (1'E,3'S)-2-(3'-acetoxy-4'-t-butyldiphenylsilyloxy-but-1'-enyl)-2-benzylmalonate(342909-14-2)
EPA Substance Registry System: dimethyl (1'E,3'S)-2-(3'-acetoxy-4'-t-butyldiphenylsilyloxy-but-1'-enyl)-2-benzylmalonate(342909-14-2)

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: 342909-14-2(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

342909-14-2 Suppliers

Recommended suppliers

342909-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 342909-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,9,0 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 342909-14:
(8*3)+(7*4)+(6*2)+(5*9)+(4*0)+(3*9)+(2*1)+(1*4)=142
142 % 10 = 2
So 342909-14-2 is a valid CAS Registry Number.

342909-14-2Upstream product

342909-14-2Downstream Products

342909-16-4 dimethyl (1'E,3'S)-2-(3',4'-dihydroxybut-1'-enyl)-2-benzylmalonate

342909-14-2Relevant academic research and scientific papers

Geminal dicarboxylates as carbonyl surrogates for asymmetric synthesis. Part II. Scope and applications

Trost,Chul Bom Lee

, p. 3687 - 3696 (2007/10/03)

An enantioselective synthesis of allylic esters has been achieved by a novel asymmetric alkylation of allylic gem-dicarboxylates. The catalyst derived from palladium(0) and R,R-1,2-di(2′-diphenylphosphinobenzamido)cyclohexene efficiently induced the alkyl

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 342909-14-2