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N-Boc-indole-2-boronic acid_Molecular_structure_CAS_213318-44-6)
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N-Boc-indole-2-boronic acid

Catalog No. 675911 Name Sigma Aldrich
CAS Number 213318-44-6 Website http://www.sigmaaldrich.com
M. F. C13H16BNO4 Telephone 1-800-521-8956
M. W. 261.08144 Fax
Purity ≥95% Email
Storage Chembase ID: 10579

SYNONYMS

Title
1-Boc-吲哚-2-硼酸
IUPAC name
{1-[(tert-butoxy)carbonyl]-1H-indol-2-yl}boronic acid
IUPAC Traditional name
1-(tert-butoxycarbonyl)indol-2-ylboronic acid
Synonyms
N-(叔丁氧基羰基)吲哚-2-硼酸
1-(tert-butoxycarbonyl)indole-2-boronic acid
N-(tert-butoxycarbonyl)indole-2-boronic acid
1-(叔丁氧基羰基)吲哚-2-硼酸

DATABASE IDS

PubChem SID 24885308
CAS Number 213318-44-6
MDL Number MFCD02093045

PROPERTIES

Empirical Formula (Hill Notation) C13H16BNO4
Purity ≥95%
Melting Point 84-94 °C
Melting Point 85-90 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Application
Used in a synthesis of hydroxyquinones via Suzuki-Miyaura coupling of phenylidonium ylides of hydroxyquinones.6
Reactant involved in:
• Suzuki-Miyaura cross-coupling reactions1,2
• Copper-catalyzed trifluoromethylation3
• Palladium-catalyzed benzylation4
• Homocoupling reactions5
General description
May contain varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Description (简体中文)
Application
用于通过羟基醌的苯基碘鎓叶立德的 Suzuki-Miyaura 偶联反应来合成羟基醌。6
Reactant involved in:
• Suzuki-Miyaura cross-coupling reactions1,2
• Copper-catalyzed trifluoromethylation3
• Palladium-catalyzed benzylation4
• Homocoupling reactions5
General description
可含有不定量的酸酐
包装
1, 5 g in glass bottle

REFERENCES