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Thiatetraphospholane, tetraphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55658-70-3

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55658-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55658-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,5 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55658-70:
(7*5)+(6*5)+(5*6)+(4*5)+(3*8)+(2*7)+(1*0)=153
153 % 10 = 3
So 55658-70-3 is a valid CAS Registry Number.

55658-70-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5-tetraphenyl-1,2,3,4,5-thiatetraphospholane

1.2 Other means of identification

Product number -
Other names 1.2.3.4-Tetraphenyl-cyclo-5-thia-1.2.3.4-tetraphosphan

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:55658-70-3 SDS

55658-70-3Downstream Products

55658-70-3Relevant academic research and scientific papers

Organosubstituted 2,5-Dihydro-1,2,5-selenasilaboroles - Preparation, Characterization, and ?-Complexation

Koester, Roland,Seidel, Guenter,Boese, Roland,Wrackmeyer, Bernd

, p. 1955 - 1966 (2007/10/02)

The dichloro compounds ClB(C2H5)CC2H5=C(R)Si(CH3)2Cl : R = CH3; B: R = C(CH3)=CH2> react with Na2Se to form the five-membered cyclic compounds .A and Na2Se2 yield 1a and 3 (2). 1a is also formed from and Se in addition to (C6H5P)n and (C6H5P)4Se (5). - (3a)2 reacts with S8 to give the compounds (7a), (4)n (n = 4,5), and (C6H5P)4S (6). - 1a reacts with CH3OH under elimination of H2Se to form the intramolecularly associated (8).From 1a and acetylacetone (9) and C5H7O2B(C2H5)SeSi(CH3)2C(CH3)=CH(C2H5) (10) are obtained. 1 : 1 Adducts are synthesised from 1a or b with Lewis acids (1a-AlCl3, 1b-AlCl3) and with Lewis bases (Py-1a, Py-1b, TMP-1a). - 1a and b react thermally or photochemically with (ligand)transition metal(0) compounds or with (ligand)transition metal(I) compounds to form η4-?-complexes 4-1a, (OC)3Ru-η4-1a, Ni(η4-1a)2 (X-ray structure analysis), C5H5Co-η4-1a, (OC)3Fe-η4-1b, (OC)3Ru-η4-1b, Ni(η4-1b)2, C5H5Co-η4-1b>.The MS and NMR data (1H, 11B, 13C, 29Si, 77Se) of the new compounds are compared with those of other C2SiElB ring compounds (El = O, S, N, P).

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