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Boranic acid dimethyl ester, also known as dimethyl borinate, is an organoborane compound with the chemical formula (CH3)2B(OH). It is a colorless, volatile liquid that is soluble in organic solvents. Boranic acid dimethyl ester is primarily used as a reagent in organic synthesis, particularly in the formation of boron-containing compounds. It can also be used as a reducing agent and a flame retardant. Boranic acid dimethyl ester is synthesized by reacting boric acid with methanol in the presence of a catalyst, such as sulfuric acid. It is important to note that Boranic acid dimethyl ester is sensitive to air and moisture, and should be stored under an inert atmosphere to prevent decomposition.

4542-61-4

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4542-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4542-61-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,4 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4542-61:
(6*4)+(5*5)+(4*4)+(3*2)+(2*6)+(1*1)=84
84 % 10 = 4
So 4542-61-4 is a valid CAS Registry Number.
InChI:InChI=1/C2H7BO2/c1-4-3-5-2/h3H,1-2H3

4542-61-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethoxyboron

1.2 Other means of identification

Product number -
Other names Dimethoxyborin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4542-61-4 SDS

4542-61-4Relevant academic research and scientific papers

Preparation of energetic poly(azolyl)borates as new environmentally benign green-light-emitting species for pyrotechnics

Klapoetke, Thomas M.,Rusan, Magdalena,Sproll, Veronique

, p. 2433 - 2443 (2013/11/19)

Three different energetic poly(azolyl)borates, potassium dihydridobis(4-nitroimidazolyl)borate, sodium dihydridobis(4, 5-dinitroimidazolyl)borate, and sodium dihydridobis(3, 4,5-trinitropyrazolyl) borate, were synthesized as starting materials for metal-f

Partial reduction of trimethoxyborane: An old reaction in a new reactor

Jeffers, Peter M.,Bauer

, p. 1698 - 1701 (2008/10/08)

Forty-fifty percent conversion of trimethoxyborane to HB(OCH3)2 was achieved by passing B(OCH3)3/H2 mixtures through a carefully controlled microwave discharge; almost all of the unconverted reactants were recovered. Similar but much less efficient reductions were obtained by exposing the reactants to focused pulses of CO2 laser radiation [P(26)-P(34) lines of the 9.6-μm band]. We were not successful in reducing trimethoxyborane by activating these mixtures with electrical discharges, with continuous, unfocused laser radiation, or via Hg-photosensitized photolysis. No significant reductions were achieved by any mode of excitation when H2S, NH3, C2H2, or CH4 replaced the H2. However, the reaction B(OCH3)3 + SiH4 = HB(OCH3)2 + SiH3(OCH3) proceeds smoothly under CW laser irradiation.

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