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32360-07-9

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32360-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32360-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,6 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 32360-07:
(7*3)+(6*2)+(5*3)+(4*6)+(3*0)+(2*0)+(1*7)=79
79 % 10 = 9
So 32360-07-9 is a valid CAS Registry Number.

32360-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1.1.1-Trimethyl-3.3-diphenyl-3-chlor-disiloxan

1.2 Other means of identification

Product number -
Other names -

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:32360-07-9 SDS

32360-07-9Relevant articles and documents

Molecular Scissors for Tailor-Made Modification of Siloxane Scaffolds

Bauer, Jonathan O.,Falk, Alexander,G?tz, Tobias

supporting information, (2021/12/09)

The controlled design of functional oligosiloxanes is an important topic in current research. A consecutive Si?O?Si bond cleavage/formation using siloxanes that are substituted with 1,2-diaminobenzene derivatives acting as molecular scissors is presented.

Reaktionen von Trimethylsiloxychlorsilanen (Me3SiO)Me2-nPhnSiCl (n = 0, 1, 2) mit Lithium - Bildung von Trimethylsiloxy-substituierten Silyl- und Disilanyllithiumverbindungen sowie Di- und Trisilanen

Harloff, Joerg,Popowski, Eckhard,Fuhrmann, Hans

, p. 136 - 146 (2007/10/03)

The trimethylsiloxychlorosilanes (Me3SiO)Me2-nPhnSiCl (1: n=0; 2: n=1; 3: n=2) were allowed to react with lithium metal in tetrahydrofuran (THF) and in a mixture of THF-diethylether-n-pentane in volume ratio 4:1:1 (Trapp mixture). The reaction of 1 with lithium metal in THF under refluxing leads to the homo-coupling product [(Me3SiO)Me2Si]2 (4). A mixture of 1 and Me3SiCl in molar ratio 1:2 reacts with lithium metal in THF to give 4 and the cross-coupling product (Me3SiO)Me2SiSiMe3 (7). The silyllithium derivatives Me3SiO(SiMePh)nLi (8: n = 1; 9: n = 2; 10: n = 3) and Me3SiSiMePhLi (11) are formed in the reaction of 2 with lithium metal in THF at -78°C and in the Trapp mixture at -110°C. Main product in both cases is 9. 8-11 are trapped by Me3SiCl and HMe2SiCl. The trapping products (Me3SiO)SiMePhSiMe3 (13a), Me3SiO(SiMePh)2SiMe2R (14a, 14b; a: R = Me, b: R = H), Me3SiO(SiMePh)3SiMe2R (15a, 15b) and Me3SiSiMePhSiMe2R (16a, 16b) are obtained. The reaction of 3 with lithium metal like 2 produces the silyllithium derivatives Me3SiO(SiPh2)nLi (18: n = 1, 19: n = 2) and Me3SiSiPh2Li (20), wich are trapped by Me3SiCl and HMe2SiCl to give the corresponding disilanes (Me3SiO)SiPh2SiMe2R (23a, 23b) and trisilanes Me3SiO(SiPh2)2SiMe2R (24a, 24b) as well as Me3SiSiPh2SiMe2R (25a, 25b). In addition to 18, 19 and 20 LiSiPh2SiPh2Li (21) is formed in a small amount in the reaction of 3 with lithium metal at -78°C to afford tetrasilanes [RMe2SiPh2Si]2 (26a, 26b) after trapping by Me3SiCl and HMe2SiCl. The disilane (Me3SiO)SiMeR′SiMe3 (17) (R′ = 3,4,5,6-tetrakis(trimethylsilyl)cyclohex-1-enyl) is produced by reaction of a mixture of 2 and Me3SiCl in molar ratio 1:6 with 6 equivalents of lithium at -78°C in THF. The reaction of a mixture of 3 and Me3SiCl in the molar ratio 1:10 with 11 equivalents of lithium under the same conditions gives (Me3SiO)SiR′2SiMe3 (27).

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