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1,3,5-Trioxa-2,4-disila-6-boracyclohexane, 2,4-dimethyl-2,4,6-triphenyl- is a complex cyclic organic compound with the molecular formula C21H21O3Si2B. 1,3,5-Trioxa-2,4-disila-6-boracyclohexane,2,4-dimethyl-2,4,6-triphenyl- is characterized by a six-membered ring structure, which includes two silicon atoms, one boron atom, and three oxygen atoms. The 2,4-dimethyl groups are attached to two of the carbon atoms in the ring, while the 2,4,6-triphenyl groups are attached to the remaining carbon atoms, providing the molecule with a highly symmetrical and stable structure. 1,3,5-Trioxa-2,4-disila-6-boracyclohexane,2,4-dimethyl-2,4,6-triphenyl- is of interest in the field of organosilicon chemistry and may have potential applications in materials science and pharmaceuticals due to its unique structure and properties.

7236-95-5

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7236-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7236-95-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,3 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7236-95:
(6*7)+(5*2)+(4*3)+(3*6)+(2*9)+(1*5)=105
105 % 10 = 5
So 7236-95-5 is a valid CAS Registry Number.

7236-95-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[carboxylatomethyl-[2-(2,6-dimethylanilino)-2-oxoethyl]amino]acetate

1.2 Other means of identification

Product number -
Other names 1,3,5-Triphenyl-3,5-dimethylcycloborodisiloxan

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:7236-95-5 SDS

7236-95-5Downstream Products

7236-95-5Relevant academic research and scientific papers

Cyclo-Boratrisiloxane and cyclo-diboratetrasiloxane derivatives and their reactions with amines: Crystal and molecular structure of (p-BrC6H4BO)2(Ph2SiO)2

Beckett, Michael A.,Hibbs, David E.,Hursthouse, Michael B.,Malik, K.M. Abdul,Owen, Paul,Varma, K. Sukumar

, p. 241 - 247 (2007/10/03)

The new cyclo-diboratetrasiloxanes (RBO)2(R′2SiO)2 (R=p-BrC6H4, o-MeC6H4, m-NH2C6H4, m-NO2C6H4, Bun;

Synthesis, properties, and ring-ring transformation reactions of cyclic siloxanes incorporating skeletal boron atoms: X-ray crystal structures of the strained boracyclotrisiloxane (PhBO)(Ph2SiO)2 and the boracyclotetrasiloxane (PhBO)(Ph2SiO)3

Foucher, Daniel A.,Lough, Alan J.,Manners, Ian

, p. 3034 - 3043 (2008/10/08)

The cyclic boratrisiloxanes (PhBO)(RR′SiO)2 (1, R = R′ = Me; 2, R = Me, R′ = Ph; 3, R = R′ = Ph) have been prepared via the reaction of the dichlorodisiloxanes 1,3-ClRR′SiOSiRR′Cl with phenylboric acid in the presence of NEt3 as an HCl acceptor. Similar procedures using the appropriate α,ω-dichlorosiloxanes ClMe2Si(OSiMe2)nOSiMe2Cl (n = 1 or 2) afforded the boracyclotetrasiloxane (PhBO)(Me2SiO)3 (4) and the boracyclopentasiloxane (PhBO)(Me2SiO)4 (5). The boracyclotetrasiloxane (PhBO)(Ph2SiO)3 (8) was isolated in low yield from the reaction of 2:1 excess of 1,3-ClPh2SiOSiPh2Cl with PhB(OH)2 in the presence of NEt3. The cyclic borasiloxanes 1 and 3 undergo extensive ring-ring transformation reactions when heated at elevated temperatures in the presence of small quantities of K[OSiMe3]. Similar reactions were detected in solution in the presence of acid or base catalysts. The products of these reactions mainly consist of larger rings containing a single boron atom, together with cyclic and polymeric siloxanes and the boroxin [PhBO]3. Similar, but slower, ring-ring redistribution reactions were detected for the boracyclotetrasiloxane 4. These results are consistent with the presence of additional strain in borasiloxanes containing a six-membered ring. This analysis was supported by a comparison of X-ray structural data obtained for 3 with that for 8. Thus, the boracyclotrisiloxane 3 was found to possess a highly strained six-membered ring with considerable bond angle distortion whereas the nonplanar eight-membered ring present in 8 is appreciably less strained. Crystals of 3 are monoclinic, space group C2/c, with a = 15.703 (6) A?, b = 10.864 (3) A?, c = 17.733 (4) A?, β = 119.14 (2)°, V = 2641 (14) A?3, and Z = 4. Crystals of 8 are monoclinic, space group P21/n, with a = 14.692 (2) A?, b = 13.707 (2) A?, c = 19.932 (3) A?, β = 111.38 (0)°, V = 3737.7 (9) A?3, and Z = 4.

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