What is the α-Tosyl-(2,4-difluorobenzyl)isocyanide?

α-Tosyl-(2,4-difluorobenzyl)isocyanide is , while it's Molecular Formula is C15H11 F2 N O2 S. Used in Organic Synthesis: α-Tosyl-(2,4-difluorobenzyl)isocyanide is used as a versatile building block for the synthesis of various organic compounds, contributing to the development of new chemical entities. Used in Pharmaceutical Industry: α-Tosyl-(2,4-difluorobenzyl)isocyanide is used as a reagent in the synthesis of pharmaceuticals, aiding in the production of drugs with potential therapeutic applications. Used in Agrochemical Industry: α-Tosyl-(2,4-difluorobenzyl)isocyanide is used as a component in the preparation of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield. Used in the Synthesis of Heterocycles: α-Tosyl-(2,4-difluorobenzyl)isocyanide is used as an effective reagent for the synthesis of various heterocycles, which are important in the development of complex molecular structures with potential applications in different fields. Safety Consideration: It is important to handle α-Tosyl-(2,4-difluorobenzyl)isocyanide with care, as isocyanides are known to be toxic and can pose a risk to human health. Proper safety measures should be implemented during its use in laboratories and industrial settings.

What is the CAS number for α-Tosyl-(2,4-difluorobenzyl)isocyanide?

The CAS number of α-Tosyl-(2,4-difluorobenzyl)isocyanide is 660431-66-3.

What is the α-Tosyl-(2,4-difluorobenzyl)isocyanide?

α-Tosyl-(2,4-difluorobenzyl)isocyanide is , while it's Molecular Formula is C15H11 F2 N O2 S. Used in Organic Synthesis: α-Tosyl-(2,4-difluorobenzyl)isocyanide is used as a versatile building block for the synthesis of various organic compounds, contributing to the development of new chemical entities. Used in Pharmaceutical Industry: α-Tosyl-(2,4-difluorobenzyl)isocyanide is used as a reagent in the synthesis of pharmaceuticals, aiding in the production of drugs with potential therapeutic applications. Used in Agrochemical Industry: α-Tosyl-(2,4-difluorobenzyl)isocyanide is used as a component in the preparation of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield. Used in the Synthesis of Heterocycles: α-Tosyl-(2,4-difluorobenzyl)isocyanide is used as an effective reagent for the synthesis of various heterocycles, which are important in the development of complex molecular structures with potential applications in different fields. Safety Consideration: It is important to handle α-Tosyl-(2,4-difluorobenzyl)isocyanide with care, as isocyanides are known to be toxic and can pose a risk to human health. Proper safety measures should be implemented during its use in laboratories and industrial settings.

What is the CAS number for α-Tosyl-(2,4-difluorobenzyl)isocyanide?

The CAS number of α-Tosyl-(2,4-difluorobenzyl)isocyanide is 660431-66-3.

Product classification

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660431-66-3

Q: What is α-Tosyl-(2,4-difluorobenzyl)isocyanide (660431-66-3) used for?

α-Tosyl-(2,4-difluorobenzyl)isocyanide is a chemical compound that features a tosyl group, a difluorobenzyl group, and an isocyanide group. It is recognized for its utility in organic synthesis, serving as a valuable building block for the creation of a diverse range of organic compounds.

Product Name:α-Tosyl-(2,4-difluorobenzyl)isocyanide
Molecular Formula:C15H11 F2 N O2 S
Molecular Weight:307.321

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Product Details

Purity:99%

99% Purity Commercial production α-Tosyl-(2,4-difluorobenzyl)isocyanide 660431-66-3 with Cheapest Price

Molecular Formula:C15H11 F2 N O2 S
Molecular Weight:307.321
PSA：42.52000
LogP:3.97650

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660431-66-3 Process route

: 668990-82-7
N-[(2.4-difluoro-phenyl)-(toluene-4-sulfonyl)-methyl]-formamide

: 660431-66-3
2,4-difluoro-1-(isocyano(tosyl)methyl)benzene

Conditions

Conditions	Yield
With triethylamine; trichlorophosphate; In tetrahydrofuran; at 0 - 10 ℃; for 1h; Inert atmosphere;	72%
With 2,6-dimethylpyridine; trichlorophosphate; In tetrahydrofuran; at 4 - 20 ℃; for 18.75h;	68%
N-[(2.4-difluoro-phenyl)-(toluene-4-sulfonyl)-methyl]-formamide; With trichlorophosphate; In tetrahydrofuran; at 20 ℃; for 0.25h; With 2,6-dimethylpyridine; at 4 - 20 ℃; for 18.5h;	68%

: 536-57-2
p-toluene sulfinic acid

: 1550-35-2
2,4-difluorobenzaldehyde

: 660431-66-3
2,4-difluoro-1-(isocyano(tosyl)methyl)benzene

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: camphor-10-sulfonic acid / 16 h / 65 - 70 °C / Inert atmosphere 2: triethylamine; trichlorophosphate / tetrahydrofuran / 1 h / 0 - 10 °C / Inert atmosphere With camphor-10-sulfonic acid; triethylamine; trichlorophosphate; In tetrahydrofuran;

660431-66-3 Upstream products

668990-82-7
N-[(2.4-difluoro-phenyl)-(toluene-4-sulfonyl)-methyl]-formamide
536-57-2
p-toluene sulfinic acid
1550-35-2
2,4-difluorobenzaldehyde

660431-66-3 Downstream products

1902955-29-6
methyl 5-(2,4-difluorophenyl)-4-methoxy-1H-pyrrole-3-carboxylate

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