Cas 558443-21-3,Carbamic acid, [(1R,4R)-4-amino-2-cyclohexen-1-yl]-, 1,1-dimethylethyl ester,

558443-21-3

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Basic information

Product Name: Carbamic acid, [(1R,4R)-4-amino-2-cyclohexen-1-yl]-, 1,1-dimethylethyl ester,
Synonyms: Carbamic acid, [(1R,4R)-4-amino-2-cyclohexen-1-yl]-, 1,1-dimethylethyl ester,
CAS NO:558443-21-3
Molecular Formula: C11H20N2O2
Molecular Weight: 212.2887
EINECS: N/A
Product Categories: N-BOC
Mol File: 558443-21-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 321.6±42.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.05±0.1 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 12.06±0.40(Predicted)
CAS DataBase Reference: Carbamic acid, [(1R,4R)-4-amino-2-cyclohexen-1-yl]-, 1,1-dimethylethyl ester,(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(1R,4R)-4-amino-2-cyclohexen-1-yl]-, 1,1-dimethylethyl ester,(558443-21-3)
EPA Substance Registry System: Carbamic acid, [(1R,4R)-4-amino-2-cyclohexen-1-yl]-, 1,1-dimethylethyl ester,(558443-21-3)

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: 558443-21-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 558443-21-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,8,4,4 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 558443-21:
(8*5)+(7*5)+(6*8)+(5*4)+(4*4)+(3*3)+(2*2)+(1*1)=173
173 % 10 = 3
So 558443-21-3 is a valid CAS Registry Number.

558443-21-3Upstream product

558443-21-3Downstream Products

558443-21-3Relevant academic research and scientific papers

Chemokine receptor binding heterocyclic compounds with enhanced efficacy

-

, (2008/06/13)

The invention relates to heterocyclic compounds consisting of a core nitrogen atom surrounded by three pendant groups, wherein two of the three pendant groups are preferably benzimidazolyl methyl and tetrahydroquinolyl, and the third pendant group contains N and optionally contains additional rings. The compounds bind to chemokine receptors, including CXCR4 and CCR5, and demonstrate protective effects against infection of target cells by a human immunodeficiency virus (HIV).

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