Cas 217944-59-7,(4S,5R,6S)-4-((S)-2-Benzyloxy-1-methyl-ethyl)-6-((R)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane

217944-59-7

Post Buying Request

Basic information

Product Name: (4S,5R,6S)-4-((S)-2-Benzyloxy-1-methyl-ethyl)-6-((R)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane
Synonyms: (4S,5R,6S)-4-((S)-2-Benzyloxy-1-methyl-ethyl)-6-((R)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane
CAS NO:217944-59-7
Molecular Formula:
Molecular Weight: 526.832
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: (4S,5R,6S)-4-((S)-2-Benzyloxy-1-methyl-ethyl)-6-((R)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R,6S)-4-((S)-2-Benzyloxy-1-methyl-ethyl)-6-((R)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane(217944-59-7)
EPA Substance Registry System: (4S,5R,6S)-4-((S)-2-Benzyloxy-1-methyl-ethyl)-6-((R)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane(217944-59-7)

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: 217944-59-7(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

217944-59-7 Suppliers

Recommended suppliers

217944-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 217944-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,9,4 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 217944-59:
(8*2)+(7*1)+(6*7)+(5*9)+(4*4)+(3*4)+(2*5)+(1*9)=157
157 % 10 = 7
So 217944-59-7 is a valid CAS Registry Number.

217944-59-7Upstream product

217944-59-7Downstream Products

217944-59-7Relevant academic research and scientific papers

Stereoselective synthesis of an isomer of membrenone-C via an aldol based two directional chain extension

Perkins, Michael V.,Sampson, Rebecca A.

, p. 8367 - 8370 (2007/10/03)

An isomer of Membrenone-C was prepared in 8 steps (17% yield) with 93% overall ds starting from the ethyl ketone (S)-10. Key steps are the boron- mediated aldol followed by anti selective reduction, giving the C6-C10 stereochemistry,

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 217944-59-7