51482-36-1 Usage
Description
(S)-A-PHTHALIMIDOPROPIONALDEHYDE is a chemical compound that belongs to the class of phthalimide derivatives. It is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. It is known for its versatile reactivity in various aromatic and heteroaromatic compounds and has potential application in the development of new drugs and materials due to its unique structural and chemical properties.
Used in Pharmaceutical Industry:
(S)-A-PHTHALIMIDOPROPIONALDEHYDE is used as a building block in organic synthesis for the development of various pharmaceuticals. Its versatile reactivity allows it to be used in the synthesis of a wide range of compounds, making it a valuable asset in the creation of new drugs.
Used in Agrochemical Industry:
(S)-A-PHTHALIMIDOPROPIONALDEHYDE is used as an intermediate in the synthesis of agrochemicals, such as the herbicide prodiamine. Its unique chemical properties make it a useful component in the development of effective and targeted agrochemicals.
Used in Fine Chemicals Industry:
(S)-A-PHTHALIMIDOPROPIONALDEHYDE is used in the synthesis of fine chemicals, including the antidepressant citalopram. Its versatility and reactivity make it a valuable component in the production of various specialty chemicals.
It is important to handle (S)-A-PHTHALIMIDOPROPIONALDEHYDE with precaution and follow strict safety measures due to its potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 51482-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,8 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51482-36:
(7*5)+(6*1)+(5*4)+(4*8)+(3*2)+(2*3)+(1*6)=111
111 % 10 = 1
So 51482-36-1 is a valid CAS Registry Number.
51482-36-1Relevant articles and documents
Effector enhanced enantioselective hydroformylation
Bai, Shao-Tao,Kluwer, Alexander M.,Reek, Joost N. H.
supporting information, p. 14151 - 14154 (2019/12/02)
In this communication, we report rhodium DIMPhos complexes with an integrated DIM-receptor that can bind carboxylate containing effectors and their application in the rhodium catalyzed hydroformylation reaction. The binding of chiral effectors in non-chiral [Rh(DIMPhos)] catalysts does not lead to enantioselective hydroformylation, but the binding of either achiral or chiral effectors can significantly enhance the enantioselectivity induced by the chiral Rh-metal complexes. For example, the supramolecular complex [Rh]/[1S?L3] displays high regio- and enantioselectivity in the hydroformylation of vinyl acetate (72% ee, and b/l >99), whereas in absence of this effector the ee is around 17%.
Iterative asymmetric hydroformylation/Wittig olefination sequence
Wong, Gene W.,Landis, Clark R.
supporting information, p. 1564 - 1567 (2013/04/24)
Over and over again: Various alkenes underwent the title reaction in the presence of rhodium/bis(diazaphospholane) complexes to give γ-chiral α,β-unsaturated carbonyl products (46-96 % yield) with high enantioselectivity (90-99 % ee). Iterative sequences
The use of nonactivated iminodienophiles in the stereoselective aza-Diels-Alder reaction
Trifonova, Anna,Andersson, Pher G.
, p. 445 - 452 (2007/10/03)
This paper describes the preparation of nitrogen-containing bicycles by the aza-Diels-Alder reaction of nonactivated iminodienophiles and cyclopentadiene. Readily available starting materials such as (S)-(-)-lactate and L-amino acids were used for the pre
