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ChemicalBook >> CAS DataBase List >>tert-Butyl 3-bromopropylcarbamate

tert-Butyl 3-bromopropylcarbamate

CAS No.
83948-53-2
Chemical Name:
tert-Butyl 3-bromopropylcarbamate
Synonyms
3-(BOC-AMINO)PROPYL BROMIDE;(3-BROMO-PROPYL)-CARBAMIC ACID TERT-BUTYL ESTER;TERT-BUTYL N-(3-BROMOPROPYL)CARBAMATE;N-BOC-3-BROMOPROPYLAMINE;N-Boc 3-broMopropan-1-aMine;N-boc-3-aminopropyl bromide;3-(BOC-amino)propyl bromide,95%;TERT-BUTYL 3-BROMOPROPYLCARBAMATE;3-(Boc-amino)propyl bromide >=96.0% (GC);N-(TERT-BUTOXYCARBONYL)-3-BROMOPROPYLAMINE
CBNumber:
CB2139373
Molecular Formula:
C8H16BrNO2
Molecular Weight:
238.12
MDL Number:
MFCD02683429
MOL File:
83948-53-2.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:52

tert-Butyl 3-bromopropylcarbamate Properties

Melting point 37-39 °C
Boiling point 285.3±23.0 °C(Predicted)
Density 1.279±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility Chloroform (Slightly), Ethyl Acetate (Sparingly), Methanol (Slightly)
pka 12.48±0.46(Predicted)
form Low Melting Solid
color White
BRN 4176344
InChI InChI=1S/C8H16BrNO2/c1-8(2,3)12-7(11)10-6-4-5-9/h4-6H2,1-3H3,(H,10,11)
InChIKey IOKGWQZQCNXXLD-UHFFFAOYSA-N
SMILES C(OC(C)(C)C)(=O)NCCCBr
CAS DataBase Reference 83948-53-2
UNSPSC Code 12352200
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P301+P312+P330-P302+P352-P305+P351+P338
Hazard Codes  Xn
Risk Statements  22-36/37/38
Safety Statements  26-24/25
WGK Germany  3
10-21
HS Code  29241990
NFPA 704
0
2 0

tert-Butyl 3-bromopropylcarbamate price More Price(37)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 17356 3-(Boc-amino)propyl bromide ≥96.0% (GC) 83948-53-2 500mg $141 2025-07-31 Buy
Sigma-Aldrich 17356 3-(Boc-amino)propyl bromide ≥96.0% (GC) 83948-53-2 2.5g $459 2025-07-31 Buy
TCI Chemical B2234 3-(tert-Butoxycarbonylamino)propyl Bromide >98.0%(T) 83948-53-2 1g $184 2025-07-31 Buy
TCI Chemical B2234 3-(tert-Butoxycarbonylamino)propyl Bromide >98.0%(T) 83948-53-2 5g $615 2025-07-31 Buy
TRC B690905 N-tert-Butoxycarbonyl-3-bromopropylamine 83948-53-2 10g $1190 2021-12-16 Buy
Product number Packaging Price Buy
17356 500mg $141 Buy
17356 2.5g $459 Buy
B2234 1g $184 Buy
B2234 5g $615 Buy
B690905 10g $1190 Buy

tert-Butyl 3-bromopropylcarbamate Chemical Properties,Uses,Production

Chemical Properties

White low melting solid

Uses

3-(Boc-amino)propyl bromide can be used as an alkylating reagent for the synthesis of:

  • Benzydamine analogs to be used as activators for soluble guanylate cyclase.
  • N-substituted chromenotriazolopyrimidine, human murine double minute 2 (MDM2) inhibitor.
  • Protected amines from piperidine derivatives to be further used for synthesis of sulfonamide series.

It can also be used for the post-polymerization quaternization of polymers to synthesize functional cationic polymers and antimicrobial agents.

reaction suitability

reagent type: cross-linking reagent

Synthesis

Di-tert-butyl dicarbonate

24424-99-5

3-Bromopropylamine hydrobromide

5003-71-4

tert-Butyl 3-bromopropylcarbamate

83948-53-2

The general procedure for the synthesis of N-Boc-3-aminopropyl bromide from di-tert-butyl dicarbonate and 3-bromopropylamine hydrobromide is as follows: refer to Example 4, Synthesis of Boc-Aminopropyl Bromide: 1.222 g (5.58 mmol) of 3-bromopropylamine hydrobromide was dissolved in 20 mL of dichloromethane to which was added under cooling in an ice bath 0.778 mL (5.58 mmol) of triethylamine and 50 mL of dichloromethane. A solution of 1.214 g (5.56 mmol) of di-tert-butyl dicarbonate (Boc2O) was added slowly and dropwise over a period of 10 min, followed by stirring of the reaction mixture. After continued stirring at room temperature for 50 min, ethyl acetate was added to the reaction system and the organic phase was washed sequentially with 5% aqueous citric acid, water and saturated saline. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent to give 1.304 g of N-Boc-3-aminopropyl bromide in 98% yield. The structure of the product was confirmed by 1H-NMR. 1H-NMR (500 MHz, CDCl3) δ (ppm) = 1.44 (9H, s, Boc group), 2.05 (2H, quintet, -NHCH2CH2CH2Br), 3.28 (2H, quartet, -NHCH2CH2CH2Br), 3.44 ( 2H, triplet, -NHCH2CH2CH2Br), 4.64 (1H, s, NH).

References

[1] Patent: EP1710257, 2006, A1
[2] Chemical Communications, 2013, vol. 49, # 51, p. 5784 - 5786
[3] Patent: EP3363463, 2018, A2. Location in patent: Paragraph 0170
[4] Patent: WO2003/99858, 2003, A1. Location in patent: Page 37
[5] Journal of Organic Chemistry, 2003, vol. 68, # 26, p. 10058 - 10066

24424-99-5
5003-71-4
83948-53-2
Synthesis of tert-Butyl 3-bromopropylcarbamate from Di-tert-butyl dicarbonate and 3-Bromopropylamine hydrobromide
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View Lastest Price from tert-Butyl 3-bromopropylcarbamate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
tert-Butyl 3-bromopropylcarbamate pictures 2025-06-09 tert-Butyl 3-bromopropylcarbamate
83948-53-2
US $213.00-198.00 / kg 1kg 98% 5mt Sach biotech Co.,Ltd
tert-Butyl 3-bromopropylcarbamate pictures 2025-04-04 tert-Butyl 3-bromopropylcarbamate
83948-53-2
US $0.00-0.00 / kg 1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
3-(Boc-amino)propylBromide pictures 2023-05-26 3-(Boc-amino)propylBromide
83948-53-2
US $0.00 / KG 0.1KG 98% 100kg Jiangsu Nata Opto-electronic Material Co.,Ltd.

tert-Butyl 3-bromopropylcarbamate Spectrum

N-(TERT-BUTOXYCARBONYL)-3-BROMOPROPYLAMINE N-(3-BROMOPROPYL)CARBAMIC ACID TERT-BUTYL ESTER N-BOC-3-BROMOPROPYLAMINE 3-(tert-Butoxycarbonylamino)propyl bromide TERT-BUTYL 3-BROMOPROPYLCARBAMATE CarbaMic acid, N-(3-broMopropyl)-, 1,1-diMethylethyl ester N-(3-Bromopropyl)carbamic Acid tert-Butyl Ester tert-Butyl N-(3-Bromopropyl)carbamate 3-(Boc-amino)propyl Bromide CarbaMic acid, (3-broMopropyl)-, 1,1-diMethylethyl ester N-Boc 3-broMopropan-1-aMine 3-(BOC-amino)propyl bromide,95% tert-butyl N-(3-broManuidylpropyl)carbaMate 3-(Boc-amino)propyl bromide >=96.0% (GC) 3-(tert-Butoxycarbonylamino)propyl Bromide N-boc-3-aminopropyl bromide 3-(tert-Butoxycarbonylamino)propyl Bromide > TERT-BUTYL N-(3-BROMOPROPYL)CARBAMATE (3-BROMO-PROPYL)-CARBAMIC ACID TERT-BUTYL ESTER 3-(BOC-AMINO)PROPYL BROMIDE 83948-53-2 BrCH23NHCO2CCH33 C8H16BrNO2 Nitrogen Compounds Organic Building Blocks Protected Amines Building Blocks