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2-(4-methoxybenzyl)-3,3-dimethylbutanoic acid is a complex organic chemical compound with the molecular formula C15H22O3. It features a butanoic acid group and a benzyl group with a methoxy substituent, making it a versatile building block in organic synthesis and pharmaceutical research for the creation of bioactive molecules and pharmaceuticals.

110577-70-3

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110577-70-3 Usage

Uses

Used in Organic Synthesis:
2-(4-methoxybenzyl)-3,3-dimethylbutanoic acid is used as a key intermediate for the synthesis of various organic compounds due to its unique structural features, which can be further modified or functionalized in chemical reactions to yield a range of products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(4-methoxybenzyl)-3,3-dimethylbutanoic acid is used as a precursor in the development of new drugs. Its complex structure allows for the exploration of its potential as a therapeutic agent or as a component in the formulation of novel pharmaceuticals, contributing to drug discovery efforts.

Check Digit Verification of cas no

The CAS Registry Mumber 110577-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,7 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 110577-70:
(8*1)+(7*1)+(6*0)+(5*5)+(4*7)+(3*7)+(2*7)+(1*0)=103
103 % 10 = 3
So 110577-70-3 is a valid CAS Registry Number.

110577-70-3Upstream product

110577-70-3Downstream Products

110577-70-3Relevant academic research and scientific papers

Structural requirements for substrate in highly enantioselective hydrogenation over the cinchonidine-modified Pd/C

Sugimura, Takashi,Uchida, Takayuki,Watanabe, Junya,Kubota, Takeshi,Okamoto, Yasuaki,Misaki, Tomonori,Okuyama, Tadashi

experimental part, p. 57 - 64 (2009/06/17)

Relationship between substrate structure and enantioselectivity is studied for the asymmetric hydrogenation of 42 different (E)-α, β-disubstituted acrylic acids (propenoic acids) over cinchonidine-modified Pd/C. The β-phenyl group is indispensable for high enantioselectivity of α-phenylcinnamic acid (2,3-diphenylpropenoic acid, 81% ee), and substitution on this group affects markedly the selectivity. The high ee up to 92% was achieved by the β - p-alkoxyphenyl substitution, and the selectivity is ascribed mainly to stronger interaction of the substrate with the chiral modifier on the catalyst surface. In contrast, substitution on the α-phenyl group does not affect notably the enantioselectivity (80-82% ee) or even the α-phenyl group itself is not indispensable but replaceable with a properly bulky group for the high enantioselectivity.

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