Cas 857732-38-8,[(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol

857732-38-8

Post Buying Request

Basic information

Product Name: [(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol
Synonyms: [(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol
CAS NO:857732-38-8
Molecular Formula:
Molecular Weight: 268.31
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: [(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol(CAS DataBase Reference)
NIST Chemistry Reference: [(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol(857732-38-8)
EPA Substance Registry System: [(2R,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-methanol(857732-38-8)

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: 857732-38-8(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

857732-38-8 Suppliers

Recommended suppliers

857732-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 857732-38-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,7,3 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 857732-38:
(8*8)+(7*5)+(6*7)+(5*7)+(4*3)+(3*2)+(2*3)+(1*8)=208
208 % 10 = 8
So 857732-38-8 is a valid CAS Registry Number.

857732-38-8Upstream product

857732-38-8Downstream Products

857732-39-9 (2S,3S,5R)-5-Methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-carboxylic acid allyl ester

857732-38-8Relevant academic research and scientific papers

Enantiospecific synthesis of the heparanase inhibitor (+)-trachyspic acid and stereoisomers from a common precursor

Zammit, Steven C.,Ferro, Vito,Hammond, Edward,Rizzacasa, Mark A.

, p. 2826 - 2834 (2007)

The total synthesis of natural (+)-trachyspic acid and its enantiomer is described starting from a common 2-deoxy-d-ribose derivative. The synthesis of the corresponding C3 epimers from the same starting material is also described. Each stereoisomer was a

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 857732-38-8