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Alpha-Naphthyl Valerate is an organic compound with the chemical formula C16H16O2. It is a derivative of alpha-naphthyl acetate, where the acetate group is replaced by a valerate group (a butanoate group). ALPHA-NAPHTHYL VALERATE is a colorless to pale yellow liquid with a characteristic odor and is soluble in organic solvents. It is primarily used as a synthetic intermediate in the production of various chemicals, pharmaceuticals, and agrochemicals. Due to its potential applications in the synthesis of drugs and other specialty chemicals, alpha-naphthyl valerate is an important compound in the field of organic chemistry.

4298-98-0

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4298-98-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4298-98-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,9 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4298-98:
(6*4)+(5*2)+(4*9)+(3*8)+(2*9)+(1*8)=120
120 % 10 = 0
So 4298-98-0 is a valid CAS Registry Number.

4298-98-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name naphthalen-1-yl pentanoate

1.2 Other means of identification

Product number -
Other names 1-Naphthyl valerate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4298-98-0 SDS

4298-98-0Relevant academic research and scientific papers

Rhodium-Catalyzed Carbonylative Coupling of Alkyl Halides with Phenols under Low CO Pressure

Ai, Han-Jun,Li, Chong-Liang,Wang, Hai,Wu, Xiao-Feng

, p. 5147 - 5152 (2020/05/27)

A rhodium-catalyzed carbonylative transformation of alkyl halides under low pressure of CO has been developed. This robust catalyst system allows using phenols as the carbonylative coupling partner and, meanwhile, exhibits high functional group tolerance and good chemoselectivity. Substrates even with a large steric hindrance group or multiple reaction sites can be selectively converted into the desired products in good to excellent yields. A gram-scale experiment was performed and delivered an almost quantitative amount of the product. Control experiments were performed as well, and a possible reaction mechanism is proposed.

Conformationally gated fragmentations and rearrangements promoted by interception of the bergman cyclization through intramolecular H-abstraction: A possible mechanism of auto-resistance to natural enediyne antibiotics?

Baroudi, Abdulkader,Mauldin, Justin,Alabugin, Igor V.

supporting information; experimental part, p. 967 - 979 (2010/03/31)

A variety of fragmentations and rearrangements can follow Bergman cyclization in enediynes equipped with acetal rings mimicking the carbohydrate moiety of natural enediyne antibiotics of the esperamicine and calchiamicine families. In the first step of all these processes, intramolecular H-atom abstraction efficiently intercepts the p-benzyne product of the Bergman cyclization through a six-membered TS and transforms the p-benzyne into a new more stable radical. Depending on the substitution pattern and reaction conditions, this radical follows four alternative paths: (a) abstraction of an external hydrogen atom, (b) O-neophyl rearrangement which transposes O- and C-atoms of the substituent, (c) fragmentation of the O-C bond in the acetal ring, or (d) fragmentation with elimination of the appended acetal moiety as a whole. Experiments with varying concentrations of external H-atom donor (1,4-cyclohexadiene) were performed to gain further insight into the competition between intermolecular H-abstraction and the fragmentations. The Thorpe-Ingold effect in gem-dimethyl substituted enediynes enhances the efficiency of fragmentation to the extent where it cannot be prevented even by a large excess of external H-atom donor. These processes provide insight into a possible mechanism of unusual fragmentation of esperamicin A1 upon its Bergman cycloaromatization and lay foundation for a new approach for the conformational control of reactivity of these natural antitumor antibiotics. Such an approach, in conjunction with supramolecular constraints, may provide a plausible mechanism for resistance to enediyne antibiotics by the enediyne-producing microorganisms.

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