90303
4-(Boc-amino)butyl bromide
technical, ≥90% (AT)
Manufacturer: Sigma Aldrich
CAS Number: 164365-88-2
Synonym(S): Carbamic acid, (4-bromobutyl)-, 1,1-dimethylethyl ester, tert-Butyl N-(4-bromobutyl)carbamate
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 500 MG | 90303-500-MG | In Stock | ₹ 8,984.75 |
| 2.5 G | 90303-2.5-G | In Stock | ₹ 36,058.08 |
90303 - 500 MG
In Stock
Quantity
1
Base Price: ₹ 8,984.75
GST (18%): ₹ 1,617.255
Total Price: ₹ 10,602.005
grade
technical
Quality Level
100
Assay
≥90% (AT)
form
liquid
reaction suitability
reagent type: cross-linking reagent
impurities
~5% 1-boc-pyrrolidine
functional group
Bocaminebromo
storage temp.
2-8°C
SMILES string
BrCCCCNC(OC(C)(C)C)=O
InChI
1S/C9H18BrNO2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7H2,1-3H3,(H,11,12)
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | eMolecules Ambeed / tert-Butyl (4-bromobutyl)carbamate / 250mg / 525023101 / A123263 / / 164365-88-2 / MFCD06201020 / 252.152 / C9H18BrNO2 | eMolecules | ₹ 2,240.82 | |
 | Sigma Aldrich Fine Chemicals Biosciences 4-(Boc-amino)butyl bromide technical, >=90% (AT) | 164365-88-2 | MFCD06201020 | 500MG | Sigma Aldrich Fine Chemicals Biosciences | ₹ 13,101.80 | |
 | eMolecules 4-(Boc-amino)butyl bromide | 164365-88-2 | 1G | Purity: 95% | eMolecules | ₹ 11,964.71 | |
 | Sigma Aldrich Fine Chemicals Biosciences 4-(Boc-amino)butyl bromide technical, >=90% (AT) | 164365-88-2 | MFCD06201020 | 2.5G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 42,814.22 | |
 | Chemscene CS-W007803,AbaChemscene,tert-Butyl (4-bromobutyl)carbamate,164365-88-2,250mg | Chemscene | ₹ 1,971.30 | |
 | Boc-NH-C4-Br | ChemScene | ₹ 684.48 - ₹ 46,373.52 |
Related Products
Description
- Application: 4-(Boc-amino)butyl bromide can be used:For the synthesis of N-Boc-aminoalkoxyphenyl derivatives, precursor to pharmacophore elements for the treatment of glaucoma.[1]For the synthesis of various aloperine derivatives with potential application as anti-HIV agents.[2]For the modification of 4,5,6,7-tetrabromobenzotriazole (TBB) derivatives to generate improved CK2 inhibitors.[3]
- Other Notes: Building block for the synthesis of natural products and biologically active compounds.[4][5]
SAFETY INFORMATION
Pictograms
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
grade: technical
Quality Level: 100
Assay: ≥90% (AT)
form: liquid
reaction suitability: reagent type: cross-linking reagent
impurities: ~5% 1-boc-pyrrolidine
functional group: Bocaminebromo
storage temp.: 2-8°C
SMILES string: BrCCCCNC(OC(C)(C)C)=O
InChI: 1S/C9H18BrNO2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7H2,1-3H3,(H,11,12)
grade:
technical
Quality Level:
100
Assay:
≥90% (AT)
form:
liquid
reaction suitability:
reagent type: cross-linking reagent
impurities:
~5% 1-boc-pyrrolidine
functional group:
Bocaminebromo
storage temp.:
2-8°C
SMILES string:
BrCCCCNC(OC(C)(C)C)=O
InChI:
1S/C9H18BrNO2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7H2,1-3H3,(H,11,12)
grade: __
Quality Level: __
Assay: __
form: powder or crystals
reaction suitability: core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalystreaction type: Cross Couplings
impurities: __
functional group: phosphine
storage temp.: __
SMILES string: __
InChI: __
grade:
__
Quality Level:
__
Assay:
__
form:
powder or crystals
reaction suitability:
core: palladiumreaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: catalystreaction type: Cross Couplings
impurities:
__
functional group:
phosphine
storage temp.:
__
SMILES string:
__
InChI:
__
grade: __
Quality Level: __
Assay: ≥95%
form: solid
reaction suitability: __
impurities: __
functional group: __
storage temp.: 2-8°C
SMILES string: __
InChI: __
grade:
__
Quality Level:
__
Assay:
≥95%
form:
solid
reaction suitability:
__
impurities:
__
functional group:
__
storage temp.:
2-8°C
SMILES string:
__
InChI:
__
grade: __
Quality Level: __
Assay: ≥95%
form: powder
reaction suitability: reagent type: catalystreaction type: Photocatalysis
impurities: __
functional group: __
storage temp.: __
SMILES string: C12=CC=CC=C1SC3=C(C=CC=C3)N2C4=CC=CC=C4
InChI: 1S/C18H13NS/c1-2-8-14(9-3-1)19-15-10-4-6-12-17(15)20-18-13-7-5-11-16(18)19/h1-13H
grade:
__
Quality Level:
__
Assay:
≥95%
form:
powder
reaction suitability:
reagent type: catalystreaction type: Photocatalysis
impurities:
__
functional group:
__
storage temp.:
__
SMILES string:
C12=CC=CC=C1SC3=C(C=CC=C3)N2C4=CC=CC=C4
InChI:
1S/C18H13NS/c1-2-8-14(9-3-1)19-15-10-4-6-12-17(15)20-18-13-7-5-11-16(18)19/h1-13H