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352359-22-9 molecular structure
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{1-[(tert-butoxy)carbonyl]-6-chloro-1H-indol-2-yl}boronic acid

ChemBase ID: 71260
Molecular Formular: C13H15BClNO4
Molecular Mass: 295.5265
Monoisotopic Mass: 295.07826605
SMILES and InChIs

SMILES:
n1(c(cc2c1cc(cc2)Cl)B(O)O)C(=O)OC(C)(C)C
Canonical SMILES:
Clc1ccc2c(c1)n(C(=O)OC(C)(C)C)c(c2)B(O)O
InChI:
InChI=1S/C13H15BClNO4/c1-13(2,3)20-12(17)16-10-7-9(15)5-4-8(10)6-11(16)14(18)19/h4-7,18-19H,1-3H3
InChIKey:
AHUWHEZTYPWOCY-UHFFFAOYSA-N

Cite this record

CBID:71260 http://www.chembase.cn/molecule-71260.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
{1-[(tert-butoxy)carbonyl]-6-chloro-1H-indol-2-yl}boronic acid
IUPAC Traditional name
1-(tert-butoxycarbonyl)-6-chloroindol-2-ylboronic acid
Synonyms
N-Boc-6-chloro-1H-indole-2-boronic acid
1-tert-Butoxycarbonyl-6-chloroindole-2-boronic acid
1-Boc-6-chloroindole-2-boronic acid
6-Chloroindole-2-boronic acid, N-BOC protected 98%
1-Boc-6-氯吲哚-2-硼酸
CAS Number
352359-22-9
MDL Number
MFCD08689539
PubChem SID
162036850
PubChem CID
44119151

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 8.205184  H Acceptors 3 
H Donor 2  LogD (pH = 5.5) 3.1856492 
LogD (pH = 7.4) 3.123628  Log P 3.1865 
Molar Refractivity 70.4476 cm3 Polarizability 30.57532 Å3
Polar Surface Area 71.69 Å2 Rotatable Bonds 3 
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
110-113°C expand Show data source
110-113°C expand Show data source
Storage Warning
IRRITANT expand Show data source
Irritant/Keep Cold expand Show data source
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
MSDS Link
Download expand Show data source
Risk Statements
36/37/38 expand Show data source
Safety Statements
26-37-60 expand Show data source
TSCA Listed
否 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Hazard statements
H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P305+P351+P338-P302+P352-P321-P405-P501A expand Show data source
Purity
98% expand Show data source

DETAILS

DETAILS

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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