Cas 824967-36-4,N-((2R,3R,4R,5S,6R)-4-Benzyloxy-5-hydroxy-6-hydroxymethyl-2-pent-4-enyloxy-tetrahydro-pyran-3-yl)-acetamide

824967-36-4

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Basic information

Product Name: N-((2R,3R,4R,5S,6R)-4-Benzyloxy-5-hydroxy-6-hydroxymethyl-2-pent-4-enyloxy-tetrahydro-pyran-3-yl)-acetamide
Synonyms: N-((2R,3R,4R,5S,6R)-4-Benzyloxy-5-hydroxy-6-hydroxymethyl-2-pent-4-enyloxy-tetrahydro-pyran-3-yl)-acetamide
CAS NO:824967-36-4
Molecular Formula:
Molecular Weight: 379.453
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: N-((2R,3R,4R,5S,6R)-4-Benzyloxy-5-hydroxy-6-hydroxymethyl-2-pent-4-enyloxy-tetrahydro-pyran-3-yl)-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((2R,3R,4R,5S,6R)-4-Benzyloxy-5-hydroxy-6-hydroxymethyl-2-pent-4-enyloxy-tetrahydro-pyran-3-yl)-acetamide(824967-36-4)
EPA Substance Registry System: N-((2R,3R,4R,5S,6R)-4-Benzyloxy-5-hydroxy-6-hydroxymethyl-2-pent-4-enyloxy-tetrahydro-pyran-3-yl)-acetamide(824967-36-4)

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: 824967-36-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 824967-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,9,6 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 824967-36:
(8*8)+(7*2)+(6*4)+(5*9)+(4*6)+(3*7)+(2*3)+(1*6)=204
204 % 10 = 4
So 824967-36-4 is a valid CAS Registry Number.

824967-36-4Upstream product

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824967-36-4Relevant academic research and scientific papers

Design and synthesis of dimeric heparinoid mimetics

Rele, Shyam M.,Iyer, Suri S.,Baskaran, Subramanian,Chaikof, Elliot L.

, p. 9159 - 9170 (2007/10/03)

Synthetic oligosaccharide constructs exhibiting tailored and well-defined heparan sulfate (HS) like sequences offer the potential to modulate dynamic HS-dependent biomolecular recognition processes. We report an efficient strategy for the generation of HS

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