64277-22-1 Usage
Description
4-(N,N-dimethylamino)butanal dimethyl acetal is an organic compound characterized by its aldehyde and acetal functional groups, along with a dimethylamino group attached to the butanal chain. This molecule is known for its reactivity and is commonly utilized as a building block in the synthesis of various organic compounds.
Uses
Used in Pharmaceutical Industry:
4-(N,N-dimethylamino)butanal dimethyl acetal is used as a reactant for the synthesis of hallucinogenic tryptamines, which are a class of compounds with psychoactive properties. These tryptamines can be employed for research purposes in understanding the mechanisms of hallucination and potentially developing new treatments for neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 64277-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,7 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64277-22:
(7*6)+(6*4)+(5*2)+(4*7)+(3*7)+(2*2)+(1*2)=131
131 % 10 = 1
So 64277-22-1 is a valid CAS Registry Number.
64277-22-1Relevant articles and documents
Process for preparation of adjacently disubstituted ketones
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, (2008/06/13)
A novel 7-hydroxyprostaglandin E1, or a stereoisomer thereof, or a protected derivative thereof, having the following formula: STR1 wherein R8 represents H, CH3 or C2 H5, R9 represents H or CH3, R10 and R11 are identical or different, and each represents H, tetrahydropyranyl or t-butyldimethylsilyl. Also provided is a process for producing an adjacently disubstituted ketone including the above compounds, i.e. 7-oxoprostaglandin, etc. which comprises reacting an α,β-unsaturated carbonyl compound with a cuprous salt and an organolithium compound in an aprotic inert organic medium in the presence of trialkylphosphine, the amounts of said cuprous salt and said organolithium compound being substantially equimolar, and reacting the product with a protected acetal derivative of an organic carbonyl compound or an aldehyde in the presence of a Lewis acid, if necessary, followed by reacting the product with a proton donor.
