5701-86-0 Usage
Uses
Used in Chemical Synthesis:
2,3-DIMETHOXY-5-METHYL-BENZALDEHYDE is used as an intermediate in the synthesis of other chemicals, leveraging its structural properties to facilitate the formation of desired products in chemical reactions.
Used in Laboratory Experiments:
As a precursor in various laboratory experiments, 2,3-DIMETHOXY-5-METHYL-BENZALDEHYDE is utilized for its reactivity and potential to yield specific outcomes in research settings.
Used in Pharmaceutical Industry:
2,3-DIMETHOXY-5-METHYL-BENZALDEHYDE is used as a building block in the development of pharmaceutical compounds, contributing to the creation of new drugs or improving existing ones.
Used in Fragrance Industry:
Due to its aromatic nature, 2,3-DIMETHOXY-5-METHYL-BENZALDEHYDE is used as a component in the formulation of fragrances, adding unique scents to various products.
Used in Dye and Pigment Industry:
2,3-DIMETHOXY-5-METHYL-BENZALDEHYDE is employed in the production of dyes and pigments, where its chemical properties contribute to the color and stability of the final products.
It is important to handle 2,3-DIMETHOXY-5-METHYL-BENZALDEHYDE with care due to potential hazards associated with exposure or reactivity, ensuring safe usage in all applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5701-86-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,0 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5701-86:
(6*5)+(5*7)+(4*0)+(3*1)+(2*8)+(1*6)=90
90 % 10 = 0
So 5701-86-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H17ClN2O5S/c1-2-26-18(23)15-11-5-3-4-6-14(11)27-17(15)20-16(22)12-9-10(19)7-8-13(12)21(24)25/h7-9H,2-6H2,1H3,(H,20,22)
5701-86-0Relevant academic research and scientific papers
Total synthesis of (±)-herbertenediol
Srikrishna,Satyanarayana
, p. 2892 - 2900 (2007/10/03)
A formal total synthesis of the sesquiterpene (±)-herbertenediol and its dimers mastigophorenes A-D has been accomplished, starting from vanillin via 2,3-dimethoxy-5-methylbenzaldehyde. A combination of Claisen rearrangement and ring-closing metathesis reactions were employed for the generation of the two vicinal quaternary carbons on a cyclopentane ring.
A New Synthesis of Anthraquinones Using Dihydro-oxazoles and Grignard Reagents Derived from Mg(Anthracene)(THF)3
Nicoletti, Teresa M.,Raston, Colin L.,Sargent, Melvyn V.
, p. 133 - 138 (2007/10/02)
A general synthesis of anthraquinones which depends on the displacement of the methoxy group from an o-methoxyaryldihydro-oxazole by a methoxy substituted benzylmagnesium chloride, generated by using a magnesium-anthracene complex, has been developed.The masked benzylbenzoic acids which result from these reactions are deprotected and then ring-closed to anthrones which on oxidation yield anthraquinones.In this way, the followeing naturally occurring anthraquinones (or derivatives thereof have been synthesized): chrysophanol (9), islandicin (19), digitopurpone (21), tri-O-methylemodin (26), and di-O-methylsoranjidiol (29).
