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Buntane-2-boronic acid

CAS No.
88496-88-2
Chemical Name:
Buntane-2-boronic acid
Synonyms
s-Butylboronic Acid;2-Butaneboronic acid;Butane-2-boronic acid;sec-Butylboronic acid;butan-2-ylboronic acid;BUNTANE-2-BORONIC ACID;n-Butane-2-boronic acid;n-Buntane-2-boronic acid;2-(But-2-yl)boronic acid;1-methylpropylboronic acid
CBNumber:
CB91473374
Molecular Formula:
C4H11BO2
Molecular Weight:
101.94
MDL Number:
MFCD06656265
MOL File:
88496-88-2.mol
MSDS File:
SDS
Last updated:2022-08-26 12:15:53

Buntane-2-boronic acid Properties

Melting point 85-89 °C
Boiling point 180.0±23.0 °C(Predicted)
Density 0.910±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
pka 10.59±0.43(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
WGK Germany  3

Buntane-2-boronic acid price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 687200 sec-Butylboronic acid ≥95% 88496-88-2 1g $69.2 2023-06-20 Buy
TRC B690638 2-Butylboronicacid 88496-88-2 1g $75 2021-12-16 Buy
AK Scientific B292 n-Buntane-2-boronicacid 88496-88-2 5g $41 2021-12-16 Buy
Biosynth Carbosynth FB147174 2-Butylboronicacid 88496-88-2 1g $57 2021-12-16 Buy
Biosynth Carbosynth FB147174 2-Butylboronicacid 88496-88-2 2g $92 2021-12-16 Buy
Product number Packaging Price Buy
687200 1g $69.2 Buy
B690638 1g $75 Buy
B292 5g $41 Buy
FB147174 1g $57 Buy
FB147174 2g $92 Buy

Buntane-2-boronic acid Chemical Properties,Uses,Production

Uses

suzuki reaction

Uses

Reactant for:• ;Preparation of alkyl- and aryl quinones via silver nitrate-catalyzed coupling with quinones1• ;Preparation of arenes by coupling reactions with aryl bromides and chlorides in the presence of palladium complexes of a (pentaphenylferrocenyl)di(tert-butyl)phosphine2

Purification Methods

Purify the acid by recrystallisation from *C6H6/pet ether and dry in vacuo. [McCusker et al. J Am Chem Soc 79 5179 1957, Beilstein 4 IV 4386.]

121-43-7
671795-46-3
88496-88-2
Synthesis of Buntane-2-boronic acid from Trimethyl borate and sec-BuMgBr, Fandachem

Buntane-2-boronic acid Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 122)Suppliers
Supplier Tel Email Country ProdList Advantage
Tianjin Xinshengjiahe Science & Technology Development Co,.Ltd
+86-86-22-87899925 +86-8618522618860 18522618860@163.com China 694 58
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886 info@dakenam.com China 15928 58
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
Wuhan Chemwish Technology Co., Ltd
027-67849912 sales@chemwish.com CHINA 10828 58
Fuxin Pharmaceutical
+86-021-021-50872116 +8613122107989 contact@fuxinpharm.com China 10297 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58

View Lastest Price from Buntane-2-boronic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
sec-Butylboronic acid pictures 2019-07-11 sec-Butylboronic acid
88496-88-2
US $3.00 / KG 1KG 99 100kg Career Henan Chemical Co
2-(But-2-yl)boronic acid Butane-2-boronic acid sec-Butylboronic acid Butane-2-boronic acid BUNTANE-2-BORONIC ACID sec-Butylboronic acid n-Butane-2-boronic acid n-Buntane-2-boronic acid 2-Butaneboronic acid butan-2-ylboronic acid 1-methylpropylboronic acid s-Butylboronic Acid Buntane-2-Boronic Acid,>97% Boronic acid, B-(1-methylpropyl)- B-(1-Methylpropyl)boronic acid sec-Butylboronic acid(contains varying amounts of Anhydride) 88496-88-2 Alkyl Boronic Acids Boronic Acids Organoborons Alkyl Boronic Acids Boronic Acids and Derivatives Heterocyclic Compounds Boronic Acids and Derivatives Chemical Synthesis Organometallic Reagents