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8-(2,2-diethoxyethoxy)-2,6-dimethyloct-2-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68298-28-2

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68298-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68298-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,9 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 68298-28:
(7*6)+(6*8)+(5*2)+(4*9)+(3*8)+(2*2)+(1*8)=172
172 % 10 = 2
So 68298-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H32O3/c1-6-18-16(19-7-2)13-17-12-11-15(5)10-8-9-14(3)4/h9,15-16H,6-8,10-13H2,1-5H3

68298-28-2SDS

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 8-(2,2-diethoxyethoxy)-2,6-dimethyloct-2-ene

1.2 Other means of identification

Product number -
Other names Citronellyloxyacetaldehyd-diaethylacetal

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:68298-28-2 SDS

68298-28-2Downstream Products

68298-28-2Relevant academic research and scientific papers

Cyclopropenation of alkylidene carbenes derived from α-silyl ketones

Li, Jingwei,Sun, Chunrui,Lee, Daesung

supporting information; experimental part, p. 6640 - 6641 (2010/07/04)

A new cyclopropanation reaction involving Cα-Si bond insertion of alkylidene carbenes derived from α-silyl ketones has been developed. This unprecedented alkylidene carbene reactivity features excellent selectivity for insertion into Cα-Si bonds rather than insertion into Cγ-H bonds or addition to,δ-double or -triple bonds. The selectivity trend clearly indicates that the α-oxygen in the tether significantly promotes Cγ-H insertion, although the Cα-Si bond insertion still competes effectively.

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