Cas 1245906-83-5,2,2-bis-(tert-butyl-dimethyl-silanyloxymethyl)-4-(4-methoxy-benzyloxy)butyraldehyde

1245906-83-5

Post Buying Request

Basic information

Product Name: 2,2-bis-(tert-butyl-dimethyl-silanyloxymethyl)-4-(4-methoxy-benzyloxy)butyraldehyde
Synonyms: 2,2-bis-(tert-butyl-dimethyl-silanyloxymethyl)-4-(4-methoxy-benzyloxy)butyraldehyde
CAS NO:1245906-83-5
Molecular Formula:
Molecular Weight: 496.835
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: 2,2-bis-(tert-butyl-dimethyl-silanyloxymethyl)-4-(4-methoxy-benzyloxy)butyraldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-bis-(tert-butyl-dimethyl-silanyloxymethyl)-4-(4-methoxy-benzyloxy)butyraldehyde(1245906-83-5)
EPA Substance Registry System: 2,2-bis-(tert-butyl-dimethyl-silanyloxymethyl)-4-(4-methoxy-benzyloxy)butyraldehyde(1245906-83-5)

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: 1245906-83-5(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1245906-83-5 Suppliers

Recommended suppliers

1245906-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1245906-83-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,9,0 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1245906-83:
(9*1)+(8*2)+(7*4)+(6*5)+(5*9)+(4*0)+(3*6)+(2*8)+(1*3)=165
165 % 10 = 5
So 1245906-83-5 is a valid CAS Registry Number.

1245906-83-5Upstream product

1245906-82-4 1-[3,3-bis-(tert-butyl-dimethyl-silanyloxymethyl)-pent-4-enyloxymethyl]-4-methoxy-benzene

1245906-83-5Downstream Products

1245906-84-6 3,3-bis-(tert-butyl-dimethyl-silanyloxymethyl)-5-(4-methoxy-benzyloxy)pentan-2-ol

1245906-83-5Relevant academic research and scientific papers

Synthesis and in vitro activity of 4′ and 5′-modified analogues of apiosyl nucleosides as potent anti-HCV agents

Li, Hua,Lee, Wonjae,Hong, Joon Hee

, p. 1104 - 1116 (2009)

Novel doubly branched apio dideoxynucleosides were synthesized starting from 1,3-dihydroxyacetone using an ozonolysis and Grignard addition as key steps, and evaluated for anti-hepatitis C virus (HCV) activity. The adenine derivative 24 showed significant

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 1245906-83-5