13002-10-3 Usage
General Description
1,1-Dibutoxypropane is a chemical compound with the formula C10H22O2. It is a colorless, slightly viscous liquid that is commonly used as a solvent in various industrial applications, such as in the production of paints, coatings, and adhesives. It is also utilized as a coupling agent and as a component in some cleaning products. Additionally, 1,1-Dibutoxypropane has been shown to have potential pesticidal properties, and it is being studied for its potential use as an agricultural chemical. However, the compound is also known to be irritant to the eyes, skin, and respiratory system, and proper safety precautions should be followed when handling it.
Check Digit Verification of cas no
The CAS Registry Mumber 13002-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,0 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13002-10:
(7*1)+(6*3)+(5*0)+(4*0)+(3*2)+(2*1)+(1*0)=33
33 % 10 = 3
So 13002-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H24O2/c1-4-7-9-12-11(6-3)13-10-8-5-2/h11H,4-10H2,1-3H3
13002-10-3Relevant articles and documents
A selective and convenient ruthenium mediated method for the synthesis of mixed acetals and orthoesters
Krompiec, Stanis?aw,Penczek, Robert,Ku?nik, Nikodem,Ma?ecki, Jan Grzegorz,Matlengiewicz, Marek
, p. 137 - 140 (2007)
Addition of alcohols and phenols to O-allyl compounds (allyl ethers and acrolein acetals), catalyzed by [RuCl2(PPh3)3], was examined. Intramolecular addition of an OH group, leading to the formation of cyclic acetals and o
Reactions of trialkylalanes with cyclic acetals and orthoformates in CH2Cl2 and ClCH2CH2Cl as solvents
Gafarova,Dekhtyar',Dekhtyar',Fatykhov,Spirikhin,Vostrikova,Zlotskii,Dokichev
, p. 1003 - 1008 (2007/10/03)
Under mild conditions, trialkylalanes (Et3Al and Bu i3Al) in chlorine-containing solvents (CH 2Cl2 or ClCH2CH2Cl) react with cyclic acetals and orthoformates to form glycol monoethers and dialkylacetals, respectively, in high yields. The 1H NMR spectroscopic data demonstrate that CH2Cl2 or ClCH2CH 2Cl interacts with Bui3Al.
