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1210700-52-9

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1210700-52-9 Usage

General Description

"(5-isopropyl-1,3-oxazol-4-yl)methanol" is a chemical compound with the molecular formula C8H11NO2. It consists of a 1,3-oxazole ring with an isopropyl group and a hydroxyl group attached to it. The compound is commonly used as a building block in organic synthesis and drug discovery. It may also have biological activities and potential applications in pharmaceuticals. As a result, it is important to understand its properties, behavior, and potential health effects to ensure safe handling and use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1210700-52-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,0,7,0 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1210700-52:
(9*1)+(8*2)+(7*1)+(6*0)+(5*7)+(4*0)+(3*0)+(2*5)+(1*2)=79
79 % 10 = 9
So 1210700-52-9 is a valid CAS Registry Number.

1210700-52-9Downstream Products

1210700-52-9Relevant articles and documents

Expanding the chemical space of sp 3-enriched 4,5-disubstituted oxazoles via synthesis of novel building blocks

Slobodyanyuk, Evgeniy Y.,Andriienko, Andrii A.,Vashchenko, Bohdan V.,Volochnyuk, Dmitriy M.,Ryabukhin, Sergey V.,Grygorenko, Oleksandr O.

, p. 421 - 434 (2019)

[Figure not available: see fulltext.] An efficient approach to the preparation of novel sp3-enriched 4,5-disubstituted oxazoles bearing a functional group at the C-4 position is described. The method commenced with synthesis of ethyl oxazole-4-carboxylates (13 examples, 63–99% yield), with subsequent function insertion to the heterocyclic core by late-stage functional group transformation. The LiBH4-mediated reduction of ethyl oxazole-4-carboxylates was the only method which could be optimized at multigram scale (up to 40 g), and its scope was demonstrated by preparation of 13 alcohols with (cyclo)alkyl, fluoroalkyl, or N-Boc-aminoalkyl moiety at the C-5 position (47–89% yield). The utility of these key intermediates was demonstrated by the preparation of chlorides (13 examples, 90–99% yield), azides (13 examples, 83–99% yield), amines (13 examples, 80–98% yield), and sulfonyl chlorides (4 examples, 68–97% yield) – advanced building blocks for synthetic and medicinal chemistry.

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