Imidazoles ∩ Sulfonyl Chlorides-Imidazoles| Ambeed

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Chemistry
Boronic acids/esters >>1,3,2-Dioxaborinane Aliphatic Borons Aromatic Borons BCAT Boric Acids MIDA Boronates Other Boronates Other Borons Oxaboroles Catalysis Chemistry >>Achiral Crown Ligands C-H Activation Carbon-Donor Ligands Chiral Carbon Ligands Chiral Crown Ligands Chiral Olefin Ligands Cross-Coupling Cross-Coupling Using Transition Metal Catalysts DACH or Trost Ligands Chemical Biology >>Conjugation Chemistry
Glycoscience Linkers and Crosslinkers Nucleic Acid Chemistry PEGylation Peptide Chemistry Photolabile Protecting Group Heterocyclic Building Blocks >>Acridines Aliphatic Heterocycles Aromatic Heterocycles Azetidines Benzimidazoles Benzisoxazoles Benzodioxans Benzofurans Benzothiazoles Inorganic reagents >>Inorganic Reagent Organic Building Blocks >>Acid Anhydrides Acyl Chlorides Alcohols
Aldehydes Aliphatic Chain Hydrocarbons Aliphatic Cyclic Hydrocarbons Alkenes Alkyls Alkynes Organometallic Reagents >>Grignard Reagents Organoarsenic Organobismuth Organoboron Organogermanium Organolithium Organomercury Organosilicon Organotin Specialty Synthesis >>Enzyme-Mediated Synthesis Fluorous Synthesis Ionic Liquids Solid Supported Synthesis Stains and Dyes >>
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Lofexidine Hydrochloride Varenicline Anti-inflammatory Agents >>Apremilast Asunaprevir ATB-346 Related Balsalazide Baricitinib Bencycloquidium Bromide Budesonide Cefiderocol Sulfate Tosylate Ceftaroline Fosamil Acetate Antibacterials >>AFN-1252 Related Alatrofloxacin Bedaquiline Fumarate Besifloxacin Brilacidin Caspofungin Acetate Cefiderocol Sulfate Tosylate Cefilavancin Ceftaroline Fosamil
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Agomelatine Agomelatine Related Allopregnanolone Related Amibegron Amitifadine Aripiprazole Related Basimglurant Befloxatone Antiemetics >>Aprepitant Aprepitant Related Dolasetron Related Dolasetron Mesylate Hydrate Fosaprepitant Dimeglumine Fosaprepitant Related Olanzapine Palonosetron Related Palonosetron Hydrochloride Antifungals >>Anidulafungin Related Cabotegravir More >>

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Chemistry Heterocyclic Building Blocks Spiroes Spiroes ∩ Epoxides

Spiroes ∩ Epoxides

Further Reading:

Typically In Stock

Purity

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99+%
99%
98+%
98%
97+%
97%
96+%
96%
95+%
95%
93%
90+%
90%

Size

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1mg
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5mg
10mg
25mg
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100mg
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1g
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Conditions to empty

Framework+−

1,3-dihydrospiro[indene-2,4'-piperidine] 1,4-dioxaspiro[4.5]decane 2,8-diazaspiro[4.5]decane 2-oxa-8-azaspiro[4.5]decane 3-phenyloxetane 6-azaspiro[3.4]octane 7-azaspiro[3.5]nonane 9,9'-spirobi[fluorene] spiro[cyclopropane-1,3'-indolin]-2'-one spiro[indene-2,4'-piperidin]-1(3H)-one spiro[indoline-3,4'-piperidine]

By Parent Nucleus+−

Acridines Aliphatic Heterocycles Aromatic Heterocycles Azetidines Benzofurans Dioxolanes Epoxides Imidazoles Imidazolidines Imidazolines Indolines Morpholines Other Aliphatic Heterocycles Other Aromatic Heterocycles Oxazines Oxazolidines Oxazolines Oxetanes Piperazines Piperidines Pyridines Pyrrolidines Quinazolines Tetrahydrofurans Tetrahydroisoquinolines Tetrahydropyrans Tetrahydroquinolines

By Functional Group+−

Alcohols Aliphatic Cyclic Hydrocarbons Alkenyls Amides Amines Aryls Bromides Carboxylic Acid Salts Carboxylic Acids Chiral Building Blocks Chlorides Esters Ethers Fluorinated Building Blocks Iodides Ketones Nitriles Nitroes Phenols Sulfamides Trifluoromethyls

By Chemical Elements+−

CFO CFNOS CClN CClFNS CNO CClOS CBrFNO CBrO CBNO CN CNO(-) CINO CClFN CBBrNO CClNO CFNS CBrNOS CBrClNO CClFNO CSi CBFKO CBrNO COS CClNS CBrOS CBr CFN CO CBNOS CIO CBrClFNO CNS CKNO CFOS CClFNOS CNOS CNO- CClO CBO CFNO CBrN CClNOS CI

B^x

C^x

N^x

O^x

F^x

Si^x

P^x

S^x

Cl^x

Br^x

I^x

Formula Weight+−

0-100(19) 100-200(2031) 200-300(3854) 300-400(1480) 400-500(290) 500-600(123) 600-700(18) 700-800(3) 900-1000(3) 1000+(3)

cLogP+−

(-50,-10] (-10,-5] (-5,-3] (-3,-2] (-2,-1] (-1,0] (0,0.5] (0.5,1] (1,1.5] (1.5,2] (2,2.5] (2.5,3] (3,3.5] (3.5,4] (4,4.5] (4.5,5] (5,5.5] (5.5,6] (6,10] (10,50]

H-Acceptors+−

0 1 2 3 4 5 6 7 9 8 10 (10,20] (20,200]

H-Donors+−

0 1 2 3 4 5 6 7 9 8 10 (10,20] (20,200]

Polar Surface Area+−

[0,10] (10,20] (20,30] (30,40] (40,50] (50,60] (60,70] (70,80] (80,90] (90,100] ＞100

Druglikeness+−

≤-20 [-20,-10] (-10,-6] (-6,-3] (-3,-1] (-1,0] (0,1] (1,2] (2,5] (5,20]

N_NCH/N_NH+−

[0,0.05] (0.05,0.1] (0.1,0.15] (0.15,0.2] (0.2,0.25] (0.25,0.3] (0.3,0.35] (0.35,0.4] (0.4,0.45] (0.45,0.5] (0.5,0.55] (0.55,0.6] (0.6,1]

sp3-Atoms+−

0 1 2 3 4 5 6 7 8 9 10 (10,20] (20,30] ＞30

Non-Aromatic Rings+−

0 1 2 3 [4,6] [7,10] ＞10

Aromatic Rings+−

0 1 2 3 [4,6] [7,10] ＞10

Rotatable Bonds+−

0 1 2 3 4 5 6 7 8 9 10 (10,20] ＞20

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