Cas 805230-35-7,Phenol, 2-[[[(1S)-1-(hydroxymethyl)-2-methylpropyl]amino]methyl]-6-methyl- (9CI)

805230-35-7

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Basic information

Product Name: Phenol, 2-[[[(1S)-1-(hydroxymethyl)-2-methylpropyl]amino]methyl]-6-methyl- (9CI)
Synonyms: Phenol, 2-[[[(1S)-1-(hydroxymethyl)-2-methylpropyl]amino]methyl]-6-methyl- (9CI)
CAS NO:805230-35-7
Molecular Formula: C13H21NO2
Molecular Weight: 223.31134
EINECS: N/A
Product Categories: METHYL
Mol File: 805230-35-7.mol

Chemical Properties

Melting Point: 71-72 °C
Boiling Point: 373.9±32.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.063±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 10.58±0.35(Predicted)
CAS DataBase Reference: Phenol, 2-[[[(1S)-1-(hydroxymethyl)-2-methylpropyl]amino]methyl]-6-methyl- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Phenol, 2-[[[(1S)-1-(hydroxymethyl)-2-methylpropyl]amino]methyl]-6-methyl- (9CI)(805230-35-7)
EPA Substance Registry System: Phenol, 2-[[[(1S)-1-(hydroxymethyl)-2-methylpropyl]amino]methyl]-6-methyl- (9CI)(805230-35-7)

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: 805230-35-7(Hazardous Substances Data)

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805230-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 805230-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,5,2,3 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 805230-35:
(8*8)+(7*0)+(6*5)+(5*2)+(4*3)+(3*0)+(2*3)+(1*5)=127
127 % 10 = 7
So 805230-35-7 is a valid CAS Registry Number.

805230-35-7Upstream product

805230-35-7Downstream Products

805230-35-7Relevant academic research and scientific papers

Synthesis of new tridentate chiral aminoalcohols by a multicomponent reaction and their evaluation as ligands for catalytic asymmetric Strecker reaction

Banphavichit, Vorawit,Bhanthumnavin, Worawan,Vilaivan, Tirayut

, p. 8727 - 8734 (2007)

A one-step, multicomponent Mannich-type reaction between phenols, paraformaldehyde, and β-aminoalcohols in the presence of LiCl afforded N-2-hydroxybenzyloxazolidines with high ortho-selectivity. Hydrolytic or reductive ring opening of the oxazolidines pr

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