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2-Chloropyridine-3-boronic acid_Molecular_structure_CAS_381248-04-0)
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2-Chloropyridine-3-boronic acid

Catalog No. 697095 Name Sigma Aldrich
CAS Number 381248-04-0 Website http://www.sigmaaldrich.com
M. F. C5H5BClNO2 Telephone 1-800-521-8956
M. W. 157.3627 Fax
Purity Email
Storage Chembase ID: 32692

SYNONYMS

Title
2-氯吡啶-3-硼酸
IUPAC name
(2-chloropyridin-3-yl)boronic acid
IUPAC Traditional name
2-chloropyridin-3-ylboronic acid
Synonyms
(2-Chloro-3-pyridyl)boronic acid
(2-Chloropyridin-3-yl)boronic acid
Dihydroxy(2-chloro-3-pyridyl)borane

DATABASE IDS

CAS Number 381248-04-0
MDL Number MFCD03094997

PROPERTIES

Empirical Formula (Hill Notation) C5H5BClNO2
Melting Point 121-134 °C
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Application
May contain varying amounts of anhydride
Reactant for:
• Synthesis of Et canthinone-3-carboxylates from Et 4-bromo-6-methoxy-1,5-naphthyridine-3-carboxylate via a Pd-catalyzed Suzuki-Miyaura coupling and a Cu-catalyzed amidation reaction1
• Preparation of arylmethylpyrrolidinylmethanols and amine derivatives via reaction with MIDA followed by Suzuki reaction with halides or amination with amines2
• Preparation of arylazabicyclooctane derivatives as potential arginine vasopressin receptor antagonists3
• Regioselective preparation of halo-oligopyridines and oligopyridines by the Suzuki-Miyaura cross-coupling reaction4
Packaging
1 g in glass bottle
250 mg in glass bottle
Description (简体中文)
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Application
可能含有不定量的酸酐
Reactant for:
• Synthesis of Et canthinone-3-carboxylates from Et 4-bromo-6-methoxy-1,5-naphthyridine-3-carboxylate via a Pd-catalyzed Suzuki-Miyaura coupling and a Cu-catalyzed amidation reaction1
• Preparation of arylmethylpyrrolidinylmethanols and amine derivatives via reaction with MIDA followed by Suzuki reaction with halides or amination with amines2
• Preparation of arylazabicyclooctane derivatives as potential arginine vasopressin receptor antagonists3
• Regioselective preparation of halo-oligopyridines and oligopyridines by the Suzuki-Miyaura cross-coupling reaction4
包装
1 g in glass bottle
250 mg in glass bottle

REFERENCES