1011-27-4 Usage
Description
Benzaldehyde, 3,5-dimethoxy-4-methyl-, also known as syringaldehyde, is a chemical compound with a molecular formula C10H12O3. It is a colorless liquid with a strong almond-like odor. Benzaldehyde, 3,5-dimethoxy-4-methylis known for its unique chemical properties and has been studied for potential applications in medicine and biology.
Used in Flavor and Fragrance Industry:
Benzaldehyde, 3,5-dimethoxy-4-methylis used as a flavoring agent for its almond-like odor, adding a distinct taste and aroma to food and beverages.
Used in Pharmaceutical Industry:
Benzaldehyde, 3,5-dimethoxy-4-methylis used as an intermediate in the synthesis of various pharmaceuticals and organic compounds, contributing to the development of new drugs and treatments.
Used in Chemical Research:
Due to its unique chemical properties, Benzaldehyde, 3,5-dimethoxy-4-methylis used in chemical research for studying its potential applications in medicine and biology, as well as for understanding its reactivity and behavior in various chemical reactions.
It is important to handle Benzaldehyde, 3,5-dimethoxy-4-methylwith care, as it can be hazardous if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 1011-27-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1011-27:
(6*1)+(5*0)+(4*1)+(3*1)+(2*2)+(1*7)=24
24 % 10 = 4
So 1011-27-4 is a valid CAS Registry Number.
1011-27-4Relevant articles and documents
Palladium-Catalyzed Cross-Coupling Synthesis of Hindered Biaryls and Terphenyls. Cocatalysis by Copper(I) Salts
Saa, Jose M.,Martorell, Gabriel
, p. 1963 - 1966 (1993)
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METHODS FOR PREPARING BIS-TETRAHYDROISOQUINOLINE-CONTAINING COMPOUNDS
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Page/Page column 64; 65; 66, (2019/02/06)
(-)-Jorumycin, ecteinascidin 743, saframycin A and related compounds, methods of preparing the same, formulations comprising the compounds, and methods of treating proliferative diseases with the same are provided.
Ortho Metalation Directed by α-Amino Alkoxides
Comins, Daniel L.,Brown, Jack D.
, p. 1078 - 1083 (2007/10/02)
The addition of aromatic aldehydes to certain lithium dialkylamides in benzene or tetrahydrofuran gave α-amino alkoxides which were ortho lithiated with excess n-butyllithium.Subsequent alkylation and hydrolysis provided ortho-substituted aromatic aldehydes via a one-pot reaction.The ortho metalation of α-amino alkoxides derived from 1- and 2-naphthaldehyde and various substituted benzaldehydes was examined.When N,N,N'-trimethylethylenediamine was used as the amine component of the α-amino alkoxide, metalation could be carried out at lower temperatures.This rate increase is due to an intramolecular TMEDA-like assisted metalation.The synthetic utility of this ortho metalation, including how varying the amine component of the α-amino alkoxide affects the regiochemistry and metalation rate, is discussed.
