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Decane, 1,1-dimethoxy-4,8-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106445-80-1

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106445-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106445-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,4 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106445-80:
(8*1)+(7*0)+(6*6)+(5*4)+(4*4)+(3*5)+(2*8)+(1*0)=111
111 % 10 = 1
So 106445-80-1 is a valid CAS Registry Number.

106445-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,8-dimethyl-1,1-dimethoxydecane

1.2 Other means of identification

Product number -
Other names 1,1-Dimethoxy-4,8-dimethyl-decane

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:106445-80-1 SDS

106445-80-1Downstream Products

106445-80-1Relevant academic research and scientific papers

Synthesis of 4(RS),8(S)-Dimethyldecanal: An Aggrigation Pheromone of Red Flour Beetles

Randad, R. S.,Kulkarni, G. H.

, p. 296 - 298 (2007/10/02)

A simple and straight forward synthesis of the pheromone 4(RS),8(S)-dimethyldecanal (IX) has been described starting from 7-hydroxycitronellal (I).

DIASTEREOTOPIC GROUP SELECTIVITY AT A PROSTEREOGENIC CARBON CENTER: SYNTHESIS OF (+/-)-SYN-4,8-DIMETHYLDECANAL

Schreiber, Stuart L.,Hulin, Bernard

, p. 4561 - 4564 (2007/10/02)

A group selective dealkylation reaction of a bridged ketal with trimethylsilyl iodide serves to control stereochemistry at carbon centers that are separated by five atoms.In combination with the iron/copper promoted fragmentation reaction of a hydroperoxi

OZONOLYSIS OF ALKENES AND REACTIONS OF POLYFUNCTIONAL COMPOUNDS. XXVIII. SYNTHESIS OF RACEMIC HOMO- AND BISHOMODIHYDROCITRONELLALS

Odinokov, V. N.,Akhmetova, V. R.,Cheskis, B. A.,Moiseenkov, A. M.,Tolstikov, G. A.

, p. 246 - 247 (2007/10/02)

A five-stage synthesis was developed for racemic 4,8-dimethylnonanal and diastereomeric 4,8-dimethyldecanal (attractants of meal worms Tribolium castaneum, T. confusum) from dimethylcyclooctadiene.

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