1427054-10-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
It is derived from pentan-3-one by attaching two bromine atoms and two hydroxyphenyl groups to the central carbon atom.
Explanation
The compound contains two bromine atoms, which are attached to the hydroxyphenyl groups.
Explanation
It is commonly used in organic synthesis due to its ability to form complex structures through reactions with other reagents.
Explanation
The compound may be used in the production of pharmaceuticals due to its unique structure and properties.
Explanation
It is known for its use as a reagent in laboratory experiments, particularly in the field of organic chemistry.
Explanation
Due to its specific structure and properties, 1,5-bis(2-bromo-5-hydroxyphenyl)pentan-3-one is of significant interest to researchers and chemists for various applications in organic chemistry.
Derivative of pentan-3-one
Yes
Bromine atoms
Two
Hydroxyphenyl groups
Two
Application in organic synthesis
Yes
Utilization in pharmaceuticals
Potential
Use as a laboratory reagent
Yes
Interest to researchers and chemists
High
Check Digit Verification of cas no
The CAS Registry Mumber 1427054-10-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,0,5 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1427054-10:
(9*1)+(8*4)+(7*2)+(6*7)+(5*0)+(4*5)+(3*4)+(2*1)+(1*0)=131
131 % 10 = 1
So 1427054-10-1 is a valid CAS Registry Number.
1427054-10-1Relevant articles and documents
Catalytic asymmetric synthetic method for chiral spirodiol derivative
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Paragraph 0215; 0216; 0217; 0218; 0219, (2017/08/02)
The invention belongs to the field of organic synthesis, and discloses a catalytic asymmetric synthetic method for a chiral spirodiol derivative. The catalytic asymmetric synthetic method comprises the following step: with chiral phosphoric acid as a catalyst, subjecting a compound as shown in a formula I in the specification and/or a compound as shown in a formula II in the specification to a reaction so as to obtain a product. In the formula I and the formula II, R1, R2, R4, R5, R6 and R7 are independently selected from any groups; and R3 is an alkyl group. The catalytic asymmetric synthetic method is a convenient, rapid and direct method for construction of a chiral spirodiol structure. The synthetic method provided by the invention has the advantages of high yield, good enantioselectivity, capability of tolerating a variety of functional groups, etc., can reduce the usage amount of the catalyst to 0.1 mol% during large-scale synthesis, and has application values in industrial production.
