Cas 866483-36-5,(1R)-1-[(3S,5R)-3-allyl-2-benzyl-3-isobutylisoxazolidin-5-yl]-2-(tert-butyldimethylsilanyloxy)ethanol

866483-36-5

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Basic information

Product Name: (1R)-1-[(3S,5R)-3-allyl-2-benzyl-3-isobutylisoxazolidin-5-yl]-2-(tert-butyldimethylsilanyloxy)ethanol
Synonyms: (1R)-1-[(3S,5R)-3-allyl-2-benzyl-3-isobutylisoxazolidin-5-yl]-2-(tert-butyldimethylsilanyloxy)ethanol
CAS NO:866483-36-5
Molecular Formula:
Molecular Weight: 433.707
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: (1R)-1-[(3S,5R)-3-allyl-2-benzyl-3-isobutylisoxazolidin-5-yl]-2-(tert-butyldimethylsilanyloxy)ethanol(CAS DataBase Reference)
NIST Chemistry Reference: (1R)-1-[(3S,5R)-3-allyl-2-benzyl-3-isobutylisoxazolidin-5-yl]-2-(tert-butyldimethylsilanyloxy)ethanol(866483-36-5)
EPA Substance Registry System: (1R)-1-[(3S,5R)-3-allyl-2-benzyl-3-isobutylisoxazolidin-5-yl]-2-(tert-butyldimethylsilanyloxy)ethanol(866483-36-5)

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: 866483-36-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 866483-36-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,4,8 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 866483-36:
(8*8)+(7*6)+(6*6)+(5*4)+(4*8)+(3*3)+(2*3)+(1*6)=215
215 % 10 = 5
So 866483-36-5 is a valid CAS Registry Number.

866483-36-5Upstream product

866483-36-5Downstream Products

866483-39-8 (1R)-1-[(3S,5R)-2-benzyl-3-(2-hydroxyethyl)-3-isobutylisoxazolidin-5-yl]ethane-1,2-diol

866483-36-5Relevant academic research and scientific papers

Stereochemical promiscuity in artificial transcriptional activators

Buhrlage, Sara J.,Brennan, Brian B.,Minter, Aaron R.,Mapp, Anna K.

, p. 12456 - 12457 (2005)

Small molecule replacements of transcriptional activation domains are highly desirable targets due to their utility as mechanistic tools and their long-term therapeutic potential for a variety of human diseases. Here, we examine the ability of amphipathic

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