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26495-91-0

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26495-91-0 Usage

Chemical Properties

Clear colorless to yellowish liquid

Check Digit Verification of cas no

The CAS Registry Mumber 26495-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,9 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26495-91:
(7*2)+(6*6)+(5*4)+(4*9)+(3*5)+(2*9)+(1*1)=140
140 % 10 = 0
So 26495-91-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H29NO3Si/c1-4-15-18(16-5-2,17-6-3)12-14-13-10-8-7-9-11-13/h13-14H,4-12H2,1-3H3

26495-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(triethoxysilylmethyl)cyclohexanamine

1.2 Other means of identification

Product number -
Other names Geniosil XL 926

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:26495-91-0 SDS

26495-91-0Relevant articles and documents

Preparation method of alpha-amino triethoxysilane

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Paragraph 0071; 0072; 0073; 0074; 0075, (2017/08/28)

The invention relates to a preparation method of alpha-amino triethoxysilane. The method comprises the following steps: (1) dissolving sodium ethoxide in a sufficient amount of organic solvent, then uniformly dropwise adding the sodium ethoxide solution into chloromethyl trichlorosilane, allowing the raw materials to react for a period of time at normal temperature after the dropwise addition is completed, carrying out normal pressure distillation to remove ethanol and insoluble substances to obtain chloromethyl triethoxysilane; (2) heating organic amine under the protection of nitrogen until boiling, and then dropwise adding the chloromethyl triethoxysilane prepared in the step (1), allowing the raw materials to react for 1-8 hours at the temperature of 70-200 DEG C after the dropwise addition is completed; filtering the reactant to remove the generated salt after the reaction is ended, distilling at normal pressure to remove the low-boiling-point substance, and then collecting the product at a proper boiling point under reduced pressure distillation, so that the alpha-amino triethoxysilane is obtained. According to the invention, no additional acid absorbent needs to be added, organic solvent is not added, so that the subsequent separation is simple, and the generation of by-products such as polysubstituted compounds of organic amines is less, the utilization rate of the amine is relatively high, and the side reaction of the reaction system is easy to control; the product purity can reach more than 95%, and the yield is over 40%.

METHOD FOR THE PRODUCTION OF SILICON COMPOUNDS CARRYING AMINO GROUPS

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Page/Page column 16, (2008/06/13)

The invention relates to a method for producing (N-organylaminoorganyl)triorganylsilanes and (N,N-diorganylaminoorganyl)triorganylsilanes from corresponding (triorganylsilylorganyl)halides and N-organylamines or N,N-diorganylamines. Also disclosed are (N-

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