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25592-09-0

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25592-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25592-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,9 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25592-09:
(7*2)+(6*5)+(5*5)+(4*9)+(3*2)+(2*0)+(1*9)=120
120 % 10 = 0
So 25592-09-0 is a valid CAS Registry Number.

25592-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-1,2,4,3,5-trithiadiborolane

1.2 Other means of identification

Product number -
Other names 3,5-dimethyl-cyclo-1,2,4-trithia-3,5-diborolane

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:25592-09-0 SDS

25592-09-0Relevant articles and documents

Contributions to the Chemistry of Boron. Part 194. Synthesis and Characterization of Mono, Bi-, and Tri-cyclic Boron-Nitrogen-Sulphur Ring Systems. Crystal Structure of 2,7,9,14-Tetrakis(diethylamino)-3,5,6,10,12,13-hexathia-1,8-diaza-2,4,7,9,11,14-hexaboratricyclo4,8> tetra...

Kendrick, Aidan,Noeth, Heinrich,Stalla, Beate,Storch, Wolfgang

, p. 1311 - 1320 (2007/10/02)

Reactions of the triborylamines N(BX2)3 (X = Cl or Br) with bis(dimethylboryl)disulphane (2) proceed via 4-dihalogenoboryl-3,5-dihalogeno-1,2,4,3,5-dithiazadiborolidines (3) to 2,8-dihalogeno-3,4,6,7-tetrathia-1-aza-2,5,8-triborabicyclo1,5> octanes (4a) and (4b).The bromo derivative (4b) reacts with additional (2) (1:1 molar ratio) to procedure impure NB3S6, but with an excess of (2) to yield a tricyclic system NB4S6(CH3).The halogen atoms in (4a) and (4b) can be substituted by methyl groups from Sn(CH3)4 as the methylating agent.Amination of compound (4a) with Sn(CH3)3 seems to proceed via the bis(diethylamino)derivative, but a new triclinic system (8) is the final product the structure of which has been determined by X-ray crystallography.U.v. and He I photoelectron spectra support n.m.r. evidence that the bicyclic rings (4) are planar 10?-electron systems.This conclusion is supported by MNDO and PPP calculations.

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