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1H-1,3,2-Diazaborole, 1,3-bis(1,1-dimethylethyl)-2,3-dihydro-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62085-92-1

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62085-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62085-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,8 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62085-92:
(7*6)+(6*2)+(5*0)+(4*8)+(3*5)+(2*9)+(1*2)=121
121 % 10 = 1
So 62085-92-1 is a valid CAS Registry Number.

62085-92-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-ditert-butyl-2-methyl-1,3,2-diazaborole

1.2 Other means of identification

Product number -
Other names 1H-1,3,2-Diazaborole,1,3-bis(1,1-dimethylethyl)-2,3-dihydro-2-methyl

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:62085-92-1 SDS

62085-92-1Relevant academic research and scientific papers

Darstellung und Eigenschaften von 1,3,2-Diazaborolin-Komplexen

Schulze, Joachim,Schmid, Guenter

, p. 495 - 504 (2007/10/02)

1,3-Di-tert-butyl-2-methyl-Δ4-1,3,2-diazaboroline (1a) and 2-methyl-1,3-bis(trimethylsilyl)-Δ4-1,3,2-diazaboroline (1b) react with (CH3CN)3Cr(CO)3 to form the diazaboroline complexes (ring)-Cr(CO)3 (2a, b).The synthesis of 2a also succeeds with Cr(CO)6 and 1a by UV-irradiation or thermically.The diazaborolines 1a and 1b serve as 6?-electron donors.In contrast, 2,4,5-trimethyl-1,3-diphenyl-Δ4-1,3,2-diazaboroline (1c) is coordinated to the Cr(CO)3 group via one of the phenyl rings (2c).P(C6H5)3 substitutes the diazaboroline in 2a to form (CO)4Cr2, whereas NO+ displaces one CO-group to give di carbonyl5-(1,3-di-tert-butyl-2-methyl-1,3,2-diazaboroline)>nitrosylchromium-hexafluorophosphate (3).Mesitylene substitutes the diazaboroline ring, while hexamethylborazine starts no reaction.As a result of IR, 1H-, 11B-, 13C-NMR as well as mass spectroscopic investigations, proposals for the molecular structures are made.

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