Interesting facts
Interesting Facts about 4-Chlorobut-2-ynyl N-(3-chlorophenyl)carbamate
4-Chlorobut-2-ynyl N-(3-chlorophenyl)carbamate is a fascinating chemical compound with diverse applications and properties that captivate the interest of chemists and researchers alike. Here are some compelling insights:
- Class of Compounds: This compound belongs to the class of carbamates, which are known for their role in agriculture as pesticides and herbicides. The versatility of carbamates makes them crucial in developing pest control strategies.
- Synthetic Applications: The *4-chlorobut-2-ynyl* group offers unique reactivity, making the compound useful in various synthetic pathways. It can be involved in cross-coupling reactions and other organic transformations, showcasing its utility in synthetic chemistry.
- Biological Activity: Compounds featuring chlorinated aromatic rings, such as *N-(3-chlorophenyl)*, often exhibit significant biological activity. They can serve as lead compounds for the development of pharmaceuticals, making them of great interest in medicinal chemistry.
- Environmental Impact: The study of carbamates, including this compound, is essential in understanding their environmental behavior. Research into their degradation pathways helps scientists evaluate their ecological impacts and the development of safer alternatives.
- Regulatory Considerations: Due to the presence of chlorine atoms, compounds like this one may face regulatory scrutiny regarding their safety and environmental effects. Understanding their mechanisms and potential risks is crucial for compliance with health and safety guidelines.
As remarked by prominent chemists, “The beauty of chemistry lies in the connections we make between diverse compounds.” The exploration of 4-chlorobut-2-ynyl N-(3-chlorophenyl)carbamate exemplifies this sentiment, as researchers uncover more about its potential uses and impacts.
In conclusion, the study of this compound not only enriches our understanding of carbamates but also highlights the intricate relationships between chemistry, biology, and the environment. The journey of scientific inquiry surrounding this compound is both challenging and rewarding, paving the way for innovations in various fields.
Synonyms
BARBAN
101-27-9
Carbyne
Barbamate
Barbane
Carbine
Chlorinat
Carbin
Neoban
Carbyne (herbicide)
4-Chlorobut-2-ynyl 3-chlorophenylcarbamate
4-chlorobut-2-yn-1-yl (3-chlorophenyl)carbamate
Fisons B25
4-Chloro-2-butynyl N-(3-chlorophenyl)carbamate
4-Chloro-2-butynyl m-chlorocarbanilate
4-Chloro-2-butynyl 3-chlorocarbanilate
Barbane [ISO-French]
RCRA waste no. U280
Barban [ANSI:BSI:ISO]
Carbamic acid, (3-chlorophenyl)-, 4-chloro-2-butynyl ester
CS-847
Barbanate
Caryne
2-Butynyl 4-chloro-m-chlorocarbanilate
4-Chlorobut-2-ynyl-m-chlorocarbanilate
HSDB 1514
Chloro-2-butynyl m-chlorocarbamate
A 980
C-847
S 847
EINECS 202-930-4
NSC 29168
4-Chloro-2-butynylm-chlorocarbanilate
EPA Pesticide Chemical Code 017601
2-Butynyl-4-chloro-m-chlorocarbanilate
BRN 2376181
m-Chlorocarbanilic acid, 4-chloro-2-butynyl ester
A980
DTXSID3041617
S847
CHEBI:33421
4-Chloro-2-butynyl meta-chlorocarbanilate
AI3-28201
Carbamic acid, N-(3-chlorophenyl)-, 4-chloro-2-butyn-1-yl ester
UNII-33306K781F
A-980
S-847
BARBAN [HSDB]
BARBAN [ISO]
BARBAN [MI]
2-Butyn-1-ol, 4-chloro-, m-chlorocarbanilate
NSC-29168
(4-Chlor-but-2-in-yl)-N-(3-chlor-phenyl)-carbamat
(4-Chloor-but-2-yn-yl)-N-(3-chloor-fenyl)-carbamaat
(4-Cloro-but-2-in-il)-N-(3-cloro-fenil)-carbammato
(3-Chlorophenyl)carbamic acid 4-chloro-2-butynyl ester
4-Chloro-2-butynyl m-chlorophenylcarbamate
4-Chloro-2-butynyl 3-chlorophenylcarbamate
33306K781F
DTXCID1021617
N-(3-Chloro phenyl)carbamate de 4-chloro 2-butynyle
Carbanilic acid, m-chloro-, 4-chloro-2-butynyl ester
Barbane (ISO-French)
4-CHLOROBUT-2-YNYL 3-CHLOROCARBANILATE
Barban (ANSI:BSI:ISO)
Caswell No. 068
4-CHLORO-2-BUTYN-1-YL N-(3-CHLOROPHENYL)CARBAMATE
4-(N-(3-CHLOROPHENYL)CARBAMOYLOXY)-1-CHLORO-2-BUTYNE
CARBANILIC ACID, M-CHLORO-, 4-CHLORO-2-BUTYNYL ESTER)
4-Chloro-2-butynyl-m-chlorocarbanilate
(4-Chloor-but-2-yn-yl)-N-(3-chloor-fenyl)-carbamaat [Dutch]
(4-Chlor-but-2-in-yl)-N-(3-chlor-phenyl)-carbamat [German]
(4-Cloro-but-2-in-il)-N-(3-cloro-fenil)-carbammato [Italian]
N-(3-Chloro phenyl) carbamate de 4-chloro 2 butynyle [French]
Barban, analytical standard
4-chlorobut-2-ynyl N-(3-chlorophenyl)carbamate
WLN: G2UU2OVMR CG
SCHEMBL59626
Chloro2butynyl mchlorocarbamate
N-(3-Chloro phenyl) carbamate de 4-chloro 2 butynyle
2Butynyl4chloromchlorocarbanilate
4Chloro2butynylmchlorocarbanilate
4Chlorobut2ynylmchlorocarbanilate
CHEMBL1570161
2Butynyl 4chloromchlorocarbanilate
4Chloro2butynyl mchlorocarbanilate
4Chloro2butynyl 3chlorocarbanilate
CS847
2-Butyn-1-ol, m-chlorocarbanilate
NSC29168
4Chloro2butynyl metachlorocarbanilate
Tox21_300669
4Chloro2butynyl mchlorophenylcarbamate
4Chlorobut2ynyl 3chlorophenylcarbamate
AKOS015904119
2Butyn1ol, 4chloro, mchlorocarbanilate
USEPA/OPP Pesticide Code: 017601
(4Chlorbut2inyl)N(3chlorphenyl)carbamat
Carbamic acid, 4-chloro-2-butynyl ester
NCGC00166272-01
NCGC00166272-02
NCGC00254577-01
(4Clorobut2inil)N(3clorofenil)carbammato
4Chloro2butynyl N(3chlorophenyl)carbamate
CAS-101-27-9
(4Chloorbut2ynyl)N(3chloorfenyl)carbamaat
Carbanilic acid, 4-chloro-2-butynyl ester
4Chloro2butynyl mchlorophenylcarbamate (8CI)
mChlorocarbanilic acid, 4chloro2butynyl ester
NS00008824
4-Chloro-2-butynyl 3-chlorophenylcarbamate #
C19059
Carbanilic acid, mchloro, 4chloro2butynyl ester
(3Chlorophenyl)carbamic acid 4chloro2butynyl ester
4-chlorobut-2-yn-1-yl N-(3-chlorophenyl)carbamate
N(3Chloro phenyl) carbamate de 4chloro 2 butynyle
Q9165259
Carbamic acid, (3chlorophenyl), 4chloro2butynyl ester
202-930-4
Solubility of 4-chlorobut-2-ynyl N-(3-chlorophenyl)carbamate
The solubility of 4-chlorobut-2-ynyl N-(3-chlorophenyl)carbamate in various solvents can greatly influence its application and behavior in different environments. Understanding its solubility characteristics is key to its use in synthesis and formulation. Here are some essential points regarding its solubility:
In conclusion, to obtain accurate predictions regarding the solubility of 4-chlorobut-2-ynyl N-(3-chlorophenyl)carbamate, one must consider its interactions with various solvents, temperature, and pH levels. As a general rule, experimental data should be collected to determine optimal solubility conditions for specific applications. Remember, "solubility is key in unlocking the potential of compounds in chemical processes."