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3-Chloro-2-tetrahydrofuranyl 4-nitrobenzoate is a chemical compound with the molecular formula C11H12ClNO5. It is a derivative of 4-nitrobenzoic acid, featuring a 3-chloro-2-tetrahydrofuran ring attached to the carboxylic acid group. 3-chloro-2-tetrahydrofuranyl 4-nitrobenzoate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs. The presence of the chloro and nitro groups in the molecule can contribute to its reactivity and functional group chemistry, making it a versatile building block in organic synthesis. The compound's structure and properties make it a subject of interest in the field of medicinal chemistry, where it may be used to develop new therapeutic agents or to study the effects of structural modifications on biological activity.

1026-80-8

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1026-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1026-80:
(6*1)+(5*0)+(4*2)+(3*6)+(2*8)+(1*0)=48
48 % 10 = 8
So 1026-80-8 is a valid CAS Registry Number.

1026-80-8Downstream Products

1026-80-8Relevant academic research and scientific papers

Facile synthesis of chiral 1,2-chlorohydrins via the ring-opening of meso-epoxides catalyzed by chiral phosphine oxides

Kotani, Shunsuke,Furusho, Haruka,Sugiura, Masaharu,Nakajima, Makoto

, p. 3075 - 3081 (2013)

The facile synthesis of chiral 1,2-chlorohydrins via the enantioselective ring-opening of meso-epoxides with silicon tetrachloride in the presence of a chiral phosphine oxide was accomplished. The chiral 1,2-chlorohydrins were also obtained from the corresponding cis-alkenes in one-pot without significant loss in the selectivity, thereby permitting easy access to the 1,2-chlorohydrins from cis-alkenes with good yields and enantioselectivities.

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