Home > Compound List > Compound details
123986-64-1 molecular structure
click picture or here to close

tert-butyl N-{[4-(hydroxymethyl)phenyl]methyl}carbamate

ChemBase ID: 77230
Molecular Formular: C13H19NO3
Molecular Mass: 237.29486
Monoisotopic Mass: 237.13649347
SMILES and InChIs

SMILES:
N(C(=O)OC(C)(C)C)Cc1ccc(cc1)CO
Canonical SMILES:
OCc1ccc(cc1)CNC(=O)OC(C)(C)C
InChI:
InChI=1S/C13H19NO3/c1-13(2,3)17-12(16)14-8-10-4-6-11(9-15)7-5-10/h4-7,15H,8-9H2,1-3H3,(H,14,16)
InChIKey:
KUEPOWVQABAWRK-UHFFFAOYSA-N

Cite this record

CBID:77230 http://www.chembase.cn/molecule-77230.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
tert-butyl N-{[4-(hydroxymethyl)phenyl]methyl}carbamate
IUPAC Traditional name
tert-butyl N-{[4-(hydroxymethyl)phenyl]methyl}carbamate
Synonyms
4-(Aminomethyl)benzyl alcohol, N-BOC protected
tert-Butyl [4-(hydroxymethyl)benzyl]carbamate 97%
(4-Hydroxymethyl-benzyl)-carbamic acid tert-butyl ester
CAS Number
123986-64-1
MDL Number
MFCD06411553
PubChem SID
162042103
PubChem CID
2794813

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 2794813 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 14.473755  H Acceptors
H Donor LogD (pH = 5.5) 1.8237618 
LogD (pH = 7.4) 1.8237618  Log P 1.8237618 
Molar Refractivity 66.2203 cm3 Polarizability 25.732416 Å3
Polar Surface Area 58.56 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
97.5-98.5°C expand Show data source
Storage Warning
Harmful/Irritant expand Show data source
Purity
97% expand Show data source
98% expand Show data source

DETAILS

DETAILS

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
    No data available
  • Searching...Please wait...

PATENTS

PATENTS

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

INTERNET

INTERNET

Baidu iconBaidu google iconGoogle