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1-PENTYL ISOCYANIDE 97 is a chemical compound characterized by its isocyanide functional group, which consists of a carbon atom triple-bonded to a nitrogen atom. It is a colorless liquid with a strong, pungent odor and is highly volatile. Due to its potential to irritate the skin, eyes, and respiratory system, it requires careful handling and adherence to safety precautions to minimize exposure and health risks.

18971-59-0

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18971-59-0 Usage

Uses

Used in Pharmaceutical Industry:
1-PENTYL ISOCYANIDE 97 is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique isocyanide functional group allows for the development of novel drug molecules with specific therapeutic properties.
Used in Agrochemical Industry:
1-PENTYL ISOCYANIDE 97 is utilized in the production of agrochemicals, specifically in the synthesis of pesticides and other crop protection agents. Its reactivity and versatility in chemical reactions contribute to the creation of effective and targeted agrochemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 18971-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,7 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18971-59:
(7*1)+(6*8)+(5*9)+(4*7)+(3*1)+(2*5)+(1*9)=150
150 % 10 = 0
So 18971-59-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H11N/c1-3-4-5-6-7-2/h3-6H2,1H3

18971-59-0 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Aldrich

  • (536202)  1-Pentylisocyanide  97%

  • 18971-59-0

  • 536202-1G

  • 645.84CNY

  • Detail

18971-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-isocyanopentane

1.2 Other means of identification

Product number -
Other names Pentane,1-isocyano

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:18971-59-0 SDS

18971-59-0Relevant academic research and scientific papers

Facile, catalyst-free cascade synthesis of sulfonyl guanidines: Via carbodiimide coupling with amines

Hazarika, Debojit,Borah, Arun Jyoti,Phukan, Prodeep

supporting information, p. 1418 - 1421 (2019/02/05)

An expeditious catalyst-free cascade coupling of N,N-dibromoarylsulfonamides with isonitriles and amines via carbodiimide intermediates has been developed. The protocol represents an elegant pathway for sulfonyl guanidines at room temperature within a short time with high yields and wide substrate scope. The carbodiimide intermediate could also be isolated in an appreciable yield.

Synthesis of Isoselenocyanates

Zakrzewski, Jerzy,Huras, Bogumi?a,Kie?czewska, Anna

, p. 85 - 96 (2015/12/26)

Isoselenocyanates were synthesized by two methods under phase-transfer conditions (50% aq NaOH, CH2Cl2, Aliquat 336); the first started from isocyanides and selenium and gave isoselenocyanates in 61-89% yields, while the second started from amines and used chloroform and selenium, by applying sequentially the Hofmann isonitrile synthesis and the addition of selenium, in 4-70% yields.

Synthesis and structure–activity relationship of α-keto amides as enterovirus 71 3C protease inhibitors

Zeng, Debin,Ma, Yuying,Zhang, Rui,Nie, Quandeng,Cui, Zhengjie,Wang, Yaxin,Shang, Luqing,Yin, Zheng

supporting information, p. 1762 - 1766 (2016/12/22)

α-Keto amide derivatives as enterovirus 71 (EV71) 3C protease (3Cpro) inhibitors have been synthesized and assayed for their biochemical and antiviral activities. structure–activity relationship (SAR) study indicated that small moieties were primarily tolerated at P1' and the introduction of para-fluoro benzyl at P2 notably improved the potency of inhibitor. Inhibitors 8v, 8w and 8x exhibited satisfactory activity (IC50= 1.32 ± 0.26 μM, 1.88 ± 0.35 μM and 1.52 ± 0.31 μM, respectively) and favorable CC50values (CC50> 100 μM). α-Keto amide may represent a good choice as a warhead for EV71 3Cproinhibitor.

Microwave-assisted synthesis of isonitriles: A general simple methodology

Porcheddu, Andrea,Giacomelli, Giampaolo,Salaris, Margherita

, p. 2361 - 2363 (2007/10/03)

(Chemical Equation Presented) A facile conversion of formamides to isonitriles under very mild conditions and microwave irradiation is described. This simple and efficient method has been applied for the synthesis of both aliphatic and aromatic isonitriles in high yields.

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