Alkyl bromides
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Filtered Search Results
eMolecules 811-93-8 | 1,2-Diamino-2-methylpropane | Combi-Blocks | MFCD00008054 | 88.154 | C4H12N2 | 98.000 | CC(C)(N)CN | 1g | 267188895
1,2-Diamino-2-methylpropane | Combi-Blocks | 811-93-8 | MFCD00008054 | 88.154 | C4H12N2 | 98.000 | CC(C)(N)CN | 1g | 267188895
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eMolecules 106-95-6 | Allyl bromide | Oakwood Chemical | MFCD00000244 | 120.977 | C3H5Br | 99.000 | BrCC=C | 500g | 625635690
Allyl bromide | Oakwood Chemical | 106-95-6 | MFCD00000244 | 120.977 | C3H5Br | 99.000 | BrCC=C | 500g | 625635690
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Matrix Scientific 10-BROMO-1-DECENE10-BROMO-1--5
10-bromo-1-decene Mf C10h19br Mw 219.17 Cas 62871-09-4 Mdl MFCD00078660
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eMolecules 126-38-5 | 1-Bromo-2,2-dimethoxypropane | Combi-Blocks | MFCD00000208 | 183.045 | C5H11BrO2 | 97.000 | COC(C)(CBr)OC | 25g | 517025907
1-Bromo-2,2-dimethoxypropane | Combi-Blocks | 126-38-5 | MFCD00000208 | 183.045 | C5H11BrO2 | 97.000 | COC(C)(CBr)OC | 25g | 517025907
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Medchemexpress LLC 1-bromooctane | 111-83-1 | MFCD00000276 | 99.0% | 193.12 g/mol | C8H17Br | 1 KG
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1-Bromooctane (n-octyl bromide) is a primary alkyl bromide commonly used as an alkylating reagent and as a substrate in nucleophilic substitution reactions. The terminal bromine acts as an effective leaving group, making the compound useful for SN2 and related synthetic transformations in organic chemistry and method development.
- Primary alkyl bromide for alkylation reactions.
- Terminal bromine provides an effective leaving group.
- Useful substrate for nucleophilic substitution studies.
- Applicable in organic synthesis and method development.
- Compatible with common laboratory handling and storage procedures.
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eMolecules 811-93-8 | 2-Methylpropane-1,2-diamine | ChemScene | MFCD00008054 | 88.154 | C4H12N2 | 98.000 | CC(C)(N)CN | 5g | 536794293
2-Methylpropane-1,2-diamine | ChemScene | 811-93-8 | MFCD00008054 | 88.154 | C4H12N2 | 98.000 | CC(C)(N)CN | 5g | 536794293
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eMolecules 4333-56-6 | Bromocyclopropane | Synthonix - Stock | MFCD00001271 | 120.977 | C3H5Br | 97.000 | BrC1CC1 | 10g | 487612137
Bromocyclopropane | Synthonix - Stock | 4333-56-6 | MFCD00001271 | 120.977 | C3H5Br | 97.000 | BrC1CC1 | 10g | 487612137
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Matrix Scientific 3-Bromo-2-methylpropene, 1458-98-6, MFCD00134155, 5g
Molecular Formula C4H7Br, Purity 95%, Molecular Weight 135.01, Boiling Point 94-95
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Aobchem Tert-butyl 3-allyl-3-cyanopiperidine-1-carboxylate | 95% | CAS 1861712-13-1 | C14H22N2O2 | 1g
Tert-butyl 3-allyl-3-cyanopiperidine-1-carboxylate | 95% | CAS 1861712-13-1 | C14H22N2O2 | 1g
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Aobchem 1-Bromo-3-cyano-2-fluorobenzene | ≥97% | CAS 840481-82-5 | C7H3BrFN | 25g
1-Bromo-3-cyano-2-fluorobenzene | ≥97% | CAS 840481-82-5 | C7H3BrFN | 25g
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eMolecules 20965-27-9 | 7-Bromoheptanenitrile | Combi-Blocks, Inc. | MFCD00001982 | 190.084 | C7H12BrN | 98.000 | BrCCCCCCC#N | 25g | 603146252
7-Bromoheptanenitrile | Combi-Blocks, Inc. | 20965-27-9 | MFCD00001982 | 190.084 | C7H12BrN | 98.000 | BrCCCCCCC#N | 25g | 603146252
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Aobchem 5-Bromo-8-ethoxyquinoline | ≥95% | CAS 101422-06-4 | C11H10BrNO | 250mg
5-Bromo-8-ethoxyquinoline | ≥95% | CAS 101422-06-4 | C11H10BrNO | 250mg
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Aobchem 1-Bromo-2-(1-bromoethyl)benzene | ≥97% | CAS 62384-31-0 | C8H8Br2 | 250mg
1-Bromo-2-(1-bromoethyl)benzene | ≥97% | CAS 62384-31-0 | C8H8Br2 | 250mg
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Aobchem 5-Bromo-1-(1-bromoethyl)-2-fluoro-3-methylbenzene | 97% | CAS 1823515-45-2 | C9H9Br2F | 10g
5-Bromo-1-(1-bromoethyl)-2-fluoro-3-methylbenzene | 97% | CAS 1823515-45-2 | C9H9Br2F | 10g
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Aobchem 2-Methyl-1-phenoxypropan-2-ol | 95% | CAS 13524-74-8 | C10H14O2 | 1g
2-Methyl-1-phenoxypropan-2-ol | 95% | CAS 13524-74-8 | C10H14O2 | 1g
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