2,4,6-トリメチルボロキシン

Trimethylboroxine

HCID 574072CAS 823-96-1

基本情報

標準SMILES
CB1OB(C)OB(C)O1
InChIKey
GBBSAMQTQCPOBF-UHFFFAOYSA-N
分子式
C3H9B3O3
平均分子量
125.5 g/mol
単同位体質量
126.08308535

名称と識別子

優先名称
Trimethylboroxine
IUPAC
2,4,6-trimethyl-1,3,5,2,4,6-trioxatriborinane
現地名
2,4,6-トリメチルボロキシン
英語名
Trimethylboroxine
分子式
C3H9B3O3
分子量
125.53

名称と別名

Trimethylboroxine823-96-1TrimethylboroxinDTXSID90341570RefChem:899827DTXCID10292651617-330-12,4,6-trimethyl-1,3,5,2,4,6-trioxatriborinanetrimethyl-1,3,5,2,4,6-trioxatriborinane2,4,6-trimethylboroxineMFCD00013354Trimethylboroxine 50% w/w soln. in THF
名称をさらに表示
トリメチルボロキシンメチルほう酸無水物メタンボロン酸無水物2,4,6-トリメチルボロキシン2,4,6-トリメチル-1,3,5-トリオキサ-2,4,6-トリボラシクロヘキサントリメチルボロキシン (約50%テトラヒドロフラン溶液)トリメチルボロキシン,50%テトラヒドロフラン溶液トリメチルボロキシン (W/W 50% SOLUTION IN THF)トリメチルボロキシン 50% W/W SOLN. IN THFトリメチルボロキシン 50% w/w soln. in THF2,4,6-トリメチル-2,4,6-トリボラ-1,3,5-トリオキサントリメチル-1,3,5,2,4,6-トリオキサトリボリナンTrimethylcyclotriboroxane2,4,6-Trimethylboroxin2,4,6-TrMETHYLBOROXINtrimethylboroxin,TRIMEETHYLBOROXINEMethylboric anhydrideTrimethylcyclotriborane
C3H9B3O3Trimethylboroxin (50% Solution in THF)Boroxin, trimethyl-2,4,6-Trimethyl-1,3,5,2,4,6-trioxatriborinane; 2,4,6-Trimethylboroxine; Methaneboronic anhydrideMethaneboronic anhydridetrimethyboroxinetrimethyl boroxintrimethylboroxaine

データベース識別子

CAS
823-96-1
PubChem CID
574072
DTXSID
DTXSID90341570
EC Number
617-330-1
Nikkaji
J375.125B

物性

構造計算による物性

極性表面積
27.7 Ų
水素結合供与体数
0
水素結合受容体数
3
回転可能結合数
0
重原子数
9

物理化学的性質

融点
38 °C · −38 °C(lit.)
沸点
78 · 78-80 °C(lit.)
比重(密度)
0.898 g/mL · 0.898 g/mL at 25 °C(lit.)
屈折率
20 · n20/D 1.362(lit.)
闪点
16 °F · 16 °F
貯蔵温度
Flammables area

化学的性質

化学的特性colorless to yellow solution

安全と法規制

GHS分類

GHS Classification · 4 件

Danger

H225 (30.3%): Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P260, P261, P264, P264+P265, P271, P280, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P319, P321, P332+P317, P362+P364, P363, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 152 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Hazard Classes and CategoriesFlam. Liq. 2 (30.3%)

安全データ

F
2-10-21
wgk
3
tsca
Yes
ridadr
UN 2924 3/PG 2
PRTR法
第一種指定化学物質
hs_code
29319090

化学と産業

応用分野

使用Trimethylboroxine is used as a derivatizing agent for GLC analysis. It is used in a diverse array of areas, including as a polymerization additive. It is also used in the preparation of CBS catalysts for asymmetric reductions.

調製方法 · 2 件

製造方法Trimethylboroxine is prepared by heating B(CH3)3 and B2O3 together in a sealed tube. The B2O3 powder is made by dehydrating H3BO3 under vacuum over P2O5 , at 220℃. The very hygro-scopic oxide is placed with strict exclusion of moisture in a 200-ml. thick-wall Pyrex tube provided with a ground joint, and a melting-point capillary is fastened to the tube just below the joint. The tube is connected to a vacuum pump and immersed in liquid nitrogen, and when a high vacuum has been established, a quantity of B(CH3)3 equivalent to 4.25 g. (0.061 mole) of B2O3 is condensed in the tube. The tube is sealed off, heated to 600℃ and kept at this temperature for six hours; in the process the contents turn into a clear, colorless liquid. When the tube has cooled down, the tip is broken under a nitrogen blanket and sealed to a tube leading to the vacuum pump. The tube is evacuated and the contents of the tube are transferred into a -78℃ trap. The crude product is purified by removing volatile contaminants at -45℃ and then distilling the product from a -10℃ trap into a receiver held at -78℃.

純化方法Possible impurity is methylboronic acid. If present, then add a few drops of conc H2SO4 and distil it immediately, then fractionate it through an efficient column. [McCusker et al. J Am Chem Soc 79 5179 1957, IR: Goubeau & Keller Z Anorg Allgem Chem 272 303 1953, Beilstein 4 IV 4378.]

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