15003-83-5

• 

• Basic information

  1. Product Name: 1,1,2,2-Tetramethyl-1,2-disilacyclohexane
  2. Synonyms: 1,1,2,2-tetramethyldisilinane
  3. CAS NO:15003-83-5
  4. Molecular Formula: C₈H₂₀Si₂
  5. Molecular Weight: 172.42
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 15003-83-5.mol
  9. Article Data: 4

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 166-167 °C
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 0.8312 g/cm3
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 1,1,2,2-Tetramethyl-1,2-disilacyclohexane(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1,1,2,2-Tetramethyl-1,2-disilacyclohexane(15003-83-5)
  11. EPA Substance Registry System: 1,1,2,2-Tetramethyl-1,2-disilacyclohexane(15003-83-5)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 15003-83-5(Hazardous Substances Data)

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• 1,1,2,2-TETRAMETHYL-1,2-DISILACYCLOHEXANECAS

  Cas No: 15003-83-5

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15003-83-5 Usage

General Description

1,1,2,2-Tetramethyl-1,2-disilacyclohexane is a chemical compound with the molecular formula C8H20Si2. It is a cyclic silicon compound with a six-membered ring containing two silicon atoms and four methyl groups attached to the ring. 1,1,2,2-Tetramethyl-1,2-disilacyclohexane is a colorless liquid at room temperature and is used as a precursor in the synthesis of various organosilicon compounds. It is also known for its potential application in the field of materials science, as it can be used to create silicon-based polymers and coatings with unique properties. 1,1,2,2-Tetramethyl-1,2-disilacyclohexane is of interest to researchers and industrial chemists for its potential contributions to the development of new materials and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 15003-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,0 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15003-83:
(7*1)+(6*5)+(5*0)+(4*0)+(3*3)+(2*8)+(1*3)=65
65 % 10 = 5
So 15003-83-5 is a valid CAS Registry Number.

15003-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	1,1,2,2-tetramethyldisilinane

1.2 Other means of identification

Product number	-
Other names	Tetramethyldisilacyclohexan

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:15003-83-5 SDS

15003-83-5Upstream product

• 34222-27-0 6,6,11,11-tetramethyl-5,6,11-trisila-spiro[4.6]undecane 
• 617-86-7 triethylsilane 
• 916501-34-3 2,2-diphenyl-1,1,3,3-tetramethyl-1,2,3-trisilacycloheptane 
• 67-56-1 methanol 
• 1192028-48-0 1,1,2,3,3-pentamethyl-2-phenyl-1,2,3-trisilacycloheptane 
• 590-82-9 Si,Si'-difluoro-Si,Si,Si',Si'-tetramethyl-Si,Si'-butanediyl-bis-silane 
• 90269-42-4 (3-butenyl)-1,1,2,2-tetramethyldisilane 
• 51043-84-6 1,1,2,2-tetramethyl-1,2-disilacyclohex-4-ene 
• 14799-64-5 2,7-Dichlor-2,7-dimethyl-2,7-disilaoctan 
• 110-52-1 1,4-dibromo-butane 
• 4342-61-4 1,2-dichlorotetramethylsilane 
• 34222-21-4 1,1,2,2,3,3-hexamethyl-[1,2,3]trisilepane 

15003-83-5Downstream Products

15003-83-5Relevant articles and documents

-

Sakurai,H. et al.

, p. 5272 - 5274 (1971)

-

SELECTIVE ON-LINE DEUTERATION IN GAS CHROMATOGRAPHY-MASS SPECTROMETRY FOR THE INVESTIGATION OF DISSOCIATIVE IONIZATION OF SILICON-CONTAINING COMPOUNDS

Mikaya, A. I.,Zaikin, V. G.,Ushakov, N. V.,Vdovin, V. M.

, p. 5 - 12 (1985)

A method for specific gas-phase deuteration of unsaturated silicon-containing compounds over pre-heterogenized Wilkinson's catalyst (a solution of (Ph3P)3RhCl in Carbowax 20M coated on Chromaton) in the reaction column connected to the mass spectrometer is described.This methode was employed to study the dissociative ionization of the corresponding saturated analogues.With the aid of the mass spectra of the dideutero derivatives thus obtained, the main electron-impact-induced reactions of 1,1-dimethyl-1-silacyclopentane, 1,1,2,2-tetramethyl-1,2-disilacyclohexane, 1-methyl-1-ethyl-1-silacyclobutane and ethyl triethoxysilane were elucidated.

Photochemistry of cyclic trisilanes: "Spring-loaded" precursors to methylphenylsilylene

Moiseev, Andrey G.,Coulais, Eugenie,Leigh, William J.

experimental part, p. 8485 - 8491 (2010/03/26)

Two new cyclic trisilanes containing a SiMePh moiety in the central position have been synthesized, and their photochemistries studied by steady-state and laser flash photolysis methods. The yield of the transient silylene SiMePh increases at the expense

Silicon-containing heterocyclic compounds I. Preparation and reactions of 1,1,2,2,-tetramethyl-1,2-disilacycloalkanes, from disilacyclopentane to disilacyclooctane

Kumada, Makoto,Tamao, Kohei,Takubo, Tadashi,Ishikawa, Mitsuo

, p. 43 - 55 (2007/10/05)

Four 1,2-disilacycloalkanes of the formula Me2SiSiMe2-(CH2)n, where n equals 3, 4, 5 and 6, have been prepared by two methods: one involves reaction of ClMe2SiSiMe2Cl with BrMg(CH2)nMgBr, the other comprises sodium/potassium condensation of ClMe2Si(CH2)nSiMe2Cl. It has been found that both the disilacyclopentane and -hexane exclusively undergo cleavage of the silicon-silicon bond when treated with concentrated sulfuric acid, whereas the disilacycloheptane gives several products in which the silicon-silicon bond has not been cleaved. The disilacyclopentane undergoes cleavage of the silicon-silicon bond when heated with 0.6 N sodium ethoxide in ethanol at 90°, while the disilacyclohexane is quite stable under the same conditions.

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