Cas 774603-70-2,5-(tert-butyldimethylsilyloxymethyl)-2-methyl-6-phenylhepta-1,6-dien-3-ol

774603-70-2

Post Buying Request

Basic information

Product Name: 5-(tert-butyldimethylsilyloxymethyl)-2-methyl-6-phenylhepta-1,6-dien-3-ol
Synonyms: 5-(tert-butyldimethylsilyloxymethyl)-2-methyl-6-phenylhepta-1,6-dien-3-ol
CAS NO:774603-70-2
Molecular Formula:
Molecular Weight: 346.585
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: 5-(tert-butyldimethylsilyloxymethyl)-2-methyl-6-phenylhepta-1,6-dien-3-ol(CAS DataBase Reference)
NIST Chemistry Reference: 5-(tert-butyldimethylsilyloxymethyl)-2-methyl-6-phenylhepta-1,6-dien-3-ol(774603-70-2)
EPA Substance Registry System: 5-(tert-butyldimethylsilyloxymethyl)-2-methyl-6-phenylhepta-1,6-dien-3-ol(774603-70-2)

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: 774603-70-2(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

774603-70-2 Suppliers

Recommended suppliers

774603-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 774603-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,4,6,0 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 774603-70:
(8*7)+(7*7)+(6*4)+(5*6)+(4*0)+(3*3)+(2*7)+(1*0)=182
182 % 10 = 2
So 774603-70-2 is a valid CAS Registry Number.

774603-70-2Upstream product

13291-18-4 isopropenylmagnesium bromide

774603-70-2Downstream Products

774603-70-2Relevant academic research and scientific papers

Synthesis and antiviral activity of novel 2′,4′-doubly branched carbocyclic nucleosides

Kim, Aihong,Hong, Joon Hee

, p. 813 - 822 (2004)

A series of 2′ and 4′-doubly branched carbocyclic nucleosides 15, 16, 17 and 18 were synthesized starting from simple acyclic ketone derivatives. The required 4′-quaternary carbon was constructed using Claisen rearrangement. In addition, the installation

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 774603-70-2