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Kemika Maikaʻi

  • trans-Ethyl 2-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate CAS:1334880-40-8

    trans-Ethyl 2-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate CAS:1334880-40-8

    ʻO ka trans-Ethyl 2-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate kahi hui i loaʻa kahi apo cyclohexane, carboxylic ester, a me ka hui amine i pale ʻia e tert-butoxycarbonyl (Boc). Ma ke ʻano he ester a me ka amine derivative i pale ʻia, loaʻa iā ia ka hiki ke komo i kekahi mau hopena pani, hoʻohui a me ka condensation. Hāʻawi ka hoʻonohonoho trans ma ke apo cyclohexane iā ia i kahi geometry ʻekolu-dimensional i wehewehe ʻia.

  • tert-butyl 1-isopropyl-6-oxopiperidin-3-ylcarbamate CAS: 2891599-72-5

    tert-butyl 1-isopropyl-6-oxopiperidin-3-ylcarbamate CAS: 2891599-72-5

    ʻO ka tert-butyl 1-isopropyl-6-oxopiperidin-3-ylcarbamate kahi hui heterocyclic e loaʻa ana kahi apo piperidine i pani ʻia me kahi hui isopropyl, ketone, a me ka hui pale tert-butoxycarbonyl. Hoʻopili kēia ʻano i nā hoʻohui nucleophilic a me nā pani ma o kāna mau ʻāpana ketone a me carbamate.

  • trans-tert-butyl 4-(2-hydroxycyclohexyl)piperazine-1-carboxylate CAS:943906-69-2

    trans-tert-butyl 4-(2-hydroxycyclohexyl)piperazine-1-carboxylate CAS:943906-69-2

    ʻO ka trans-tert-butyl 4-(2-hydroxycyclohexyl)piperazine-1-carboxylate kahi molekala e loaʻa ana kahi apo piperazine i pani ʻia me kahi tert-butyl carbamate a me ka waiʻona cyclohexyl. ʻAe kēia ʻano hana i ke komo ʻana i nā ʻano hoʻololi like ʻole, oxidation a me nā hopena hoʻohui ma o kāna mau hui hana reactive.

  • 2,2,2-trifluoro-1-(6-methoxy-1H-indol-3-yl)ethan-1-one CAS:676476-94-1

    2,2,2-trifluoro-1-(6-methoxy-1H-indol-3-yl)ethan-1-one CAS:676476-94-1

    ʻO 2,2,2-Trifluoro-1-(6-methoxy-1H-indol-3-yl)ethan-1-one kahi hui kemika e hana ana ma ke ʻano he waena i ka synthesis organik. Loaʻa iā ia kahi apo indole a me kahi hui trifluoroacetyl e hiki ai iā ia ke komo i nā hopena e like me ka nucleophilic substitution a me ka oxidation-reduction. Hoʻāla ka hui trifluoroacetyl i ka alpha carbon no nā hopena me nā nucleophiles ikaika ma lalo o nā kūlana akahai.

  • ʻOctahydrocyclopenta[b][1,4]oxazine hydrochloride CAS:1616436-40-8 1197767-62-6

    ʻOctahydrocyclopenta[b][1,4]oxazine hydrochloride CAS:1616436-40-8 1197767-62-6

    ʻO Octahydrocyclopenta[b][1,4]oxazine hydrochloride kahi ʻōnaehana heterocyclic i hoʻopili ʻia me kahi oxygen heterocycle i hoʻohui ʻia i kahi apo cyclopentane. Ke komo nei kēia paʻakai i nā ʻano hoʻololi like ʻole, hoʻohui a me nā hopena condensation ma o ka ʻōnaehana nitrogen kumu a me ke apo reactive.

  • 2-tert-butyl 8-methyl 5-amino-3,4-dihydroisoquinoline-2,8(1H)-dicarboxylate CAS:2757925-41-8

    2-tert-butyl 8-methyl 5-amino-3,4-dihydroisoquinoline-2,8(1H)-dicarboxylate CAS:2757925-41-8

    ʻO 2-tert-butyl 8-methyl 5-amino-3,4-dihydroisoquinoline-2,8(1H)-dicarboxylate kahi scaffold heterocyclic e loaʻa ana kahi ʻōnaehana isoquinoline i pani ʻia me nā ʻāpana amino, methyl, a me tert-butyl ester. Hoʻopili kēia ʻano hana kikoʻī i nā hoʻohui nucleophilic versatile, nā pani a me nā hopena decarboxylations ma o kāna mau hui hana reactive.

  • methyl 1-(4-bromophenyl)-3,3-dimethoxycyclobutanecarboxylate CAS:2273863-76-4

    methyl 1-(4-bromophenyl)-3,3-dimethoxycyclobutanecarboxylate CAS:2273863-76-4

    ʻO ka methyl 1-(4-bromophenyl)-3,3-dimethoxycyclobutanecarboxylate he ester cyclic e loaʻa ana kahi apo cyclobutane i hoʻohui ʻia i kahi hui bromophenyl a pani ʻia me ʻelua mau hui methoxy a me kahi methyl ester. ʻAe kēia ʻano paʻakikī i ke komo ʻana i nā ʻano cyclization, substitution, addition a me nā ester hydrolysis reactions ma o kona mau wahi reactive.

  • 3-(2-Fluoro-phenyl)-isoxazole-5-carbaldehyde CAS:808740-52-5

    3-(2-Fluoro-phenyl)-isoxazole-5-carbaldehyde CAS:808740-52-5

    ʻO 3-(2-Fluoro-phenyl)-isoxazole-5-carbaldehyde kahi aldehyde heterocyclic e loaʻa ana kahi apo isoxazole i hoʻohui ʻia i kahi apo benzene fluorinated. ʻO ke alo o nā formyl a me nā fluoro substituents e ʻae i ka reactivity like ʻole. Ma ke ʻano he isoxazole derivative, hiki iā ia ke komo i nā hopena pani a me ka hoʻohui ma ka ʻōnaehana heterocyclic. Hāʻawi ka hui hana aldehyde i nā manawa kūpono no nā ala condensation he nui.

  • 7-Methoxyquinolin-3-amine CAS:87199-83-5

    7-Methoxyquinolin-3-amine CAS:87199-83-5

    ʻO 7-Methoxyquinolin-3-amine kahi amine ʻala e loaʻa ana kahi apo quinoline me kahi methoxy a me ka amine substituent. ʻO ka hui methoxy hāʻawi electron e hoʻolilo i ka ʻōnaehana quinoline i maʻalahi i ka hoʻololi ʻala electrophilic. I kēia manawa, hāʻawi ka hui amine i nā manawa kūpono no ka kemika nucleophilic. ʻAe kēia mau hana i nā ala hana like ʻole no ka hoʻololi ʻana i ke ʻano a me ka hoʻomālamalama ʻana.

  • 7-Methoxyquinolin-3-amine CAS:87199-83-5

    7-Methoxyquinolin-3-amine CAS:87199-83-5

    ʻO 7-Methoxyquinolin-3-amine kahi amine ʻala e loaʻa ana kahi apo quinoline me kahi methoxy a me ka amine substituent. ʻO ka hui methoxy hāʻawi electron e hoʻolilo i ka ʻōnaehana quinoline i maʻalahi i ka hoʻololi ʻala electrophilic. I kēia manawa, hāʻawi ka hui amine i nā manawa kūpono no ka kemika nucleophilic. ʻAe kēia mau hana i nā ala hana like ʻole no ka hoʻololi ʻana i ke ʻano a me ka hoʻomālamalama ʻana.

  • ʻO ka Methyl 2-(1,4-diazepan-1-yl)acetate hydrochloride CAS:926223-03-2

    ʻO ka Methyl 2-(1,4-diazepan-1-yl)acetate hydrochloride CAS:926223-03-2

    ʻO Methyl 2-(1,4-diazepan-1-yl)acetate hydrochloride kahi paʻakai e loaʻa ana kahi methyl ester i hoʻopili ʻia i kahi apo 1,4-diazepane. Hoʻopili kēia ʻano hana i nā hopena hoʻololi nucleophilic a me nā hopena hoʻohui ma o ka diazepane nitrogen kumu a me ka ester hydrolysis ma ka carboxylate.

  • ʻEthyl trans-2-amino-1-cyclohexanecarboxylate hydrochloride CAS:28250-14-8

    ʻEthyl trans-2-amino-1-cyclohexanecarboxylate hydrochloride CAS:28250-14-8

    ʻO Ethyl trans-2-amino-1-cyclohexanecarboxylate hydrochloride kahi hui organik e loaʻa ana kahi hui hana amino a me ka carboxylic ester. Aia ia ma ke ʻano he paʻakai paʻa keʻokeʻo i hana ʻia ma waena o ka waikawa hydrochloric a me ka hui amino o ka molekole makua. ʻO ka hoʻonohonoho trans a puni ka amino substituent e hāʻawi iā ia i kahi ʻano ʻekolu-dimensional i wehewehe ʻia. Hiki i kēia hui ke komo i nā ʻano hoʻololi like ʻole, hoʻohui a me nā hopena condensation ma muli o ka reactivity o nā hui amino a me carboxylic ester.