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(3,4-Dichloro-phenoxy)-acetonitrile is a synthetic chemical compound that serves as an intermediate in the production of various commercial products, including pharmaceuticals, agricultural chemicals, and dyes. It is a white to light brown solid at room temperature, insoluble in water, and soluble in organic solvents. Due to its toxic nature, it is crucial to handle this chemical with care to prevent adverse health effects.

38949-69-8

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38949-69-8 Usage

Uses

Used in Pharmaceutical Industry:
(3,4-Dichloro-phenoxy)-acetonitrile is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its role in drug development is essential, as it contributes to the creation of medications that address a range of health conditions.
Used in Agricultural Chemical Industry:
In the agricultural sector, (3,4-Dichloro-phenoxy)-acetonitrile is utilized as an intermediate in the production of agricultural chemicals. These chemicals may include pesticides or herbicides that are vital for protecting crops and ensuring a stable food supply.
Used in Dye Industry:
(3,4-Dichloro-phenoxy)-acetonitrile is also employed as an intermediate in the manufacturing of dyes. This application is significant for the textile industry, where dyes are used to color fabrics and create a diverse range of products.
Safety Precautions:
Given the toxic and harmful properties of (3,4-Dichloro-phenoxy)-acetonitrile, it is imperative to follow proper safety protocols and guidelines when working with or handling this chemical. This includes taking measures to prevent ingestion, inhalation, or skin contact to ensure the well-being of individuals in its vicinity.

Check Digit Verification of cas no

The CAS Registry Mumber 38949-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,9,4 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38949-69:
(7*3)+(6*8)+(5*9)+(4*4)+(3*9)+(2*6)+(1*9)=178
178 % 10 = 8
So 38949-69-8 is a valid CAS Registry Number.

38949-69-8Relevant academic research and scientific papers

Synthesis of aryloxyacetonitriles based on arylboronic acids with 2-bromoacetonitrile

Li, Yingmin,Guo, Mengping,Wen, Yongju,Zhou, Lanjiang,Shen, Xiuli,Kang, Yangping

supporting information, (2020/09/09)

A new and efficient protocol for the synthesis of aryloxyacetonitriles based on arylboronic acids with 2-bromoacetonitrile has been developed using eco-friendly hydrogen peroxide as oxidant under metal-free conditions. This method is compatible with arylboronic acid attached sensitive substituent and obtains desired product in moderate to good yield.

MODULATORS OF THE INTEGRATED STRESS PATHWAY

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Page/Page column 139, (2019/05/22)

Provided herein are compounds, compositions, and methods useful for modulating the integrated stress response (ISR) and for treating related diseases; disorders and conditions.

MODULATORS OF THE INTEGRATED STRESS PATHWAY

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Page/Page column 134, (2017/12/13)

Provided herein are compounds, compositions, and methods useful for modulating the integrated stress response (ISR) and for treating related diseases; disorders and conditions.

Effect of Methoxy Substitution on the Adrenergic Activity of Three Structurally Related α2-Adrenoreceptor Antagonists

Stillings, Michael R.,England, C. David,Welbourn, Anthony P.,Smith, Colin F. C.

, p. 1780 - 1783 (2007/10/02)

We have recently reported the synthesis and α2-antagonist activity of the methoxy derivative 2 and described the enhanced potency of this compound over the parent 1,4-benzodioxan, idazoxan, in

Composition and process for promoting the growth of crop plants

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, (2008/06/13)

Compounds of the formula wherein Ar is (substituted) phenyl or naphthyl, X is oxygen, sulfur, SO or SO2, n is 1-3 and R is CN or C(NH2)NOR1, (wherein R1 is preferably hydrogen) are useful as safeners in crop protection.

Method of inhibiting sickling of sickle erythrocytes using substituted-2-imidazolines

-

, (2008/06/13)

Method for inhibiting the sickling of sickle erythrocytes in blood by contacting the sickle erythrocytes with a compound of the formula: STR1 or a pharmaceutically-acceptable salt thereof, wherein X represents sulfur, oxygen or imino; Rm represents chloro, bromo, fluoro or iodo; and Rp represents chloro, bromo, fluoro, iodo, hydroxy, amino or alkyl.

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