15408

N-Boc-1,3-propanediamine

≥97.0% (GC/NT)

Manufacturer: Sigma Aldrich

CAS Number: 75178-96-0

Synonym(S): N-Boc-1,3-diaminopropane, tert-Butyl N-(3-aminopropyl)carbamate

Select a Size

Pack Size SKU Availability Price
1 ML 15408-1-ML In Stock ₹ 6,884.70
5 ML 15408-5-ML In Stock ₹ 27,203.23

15408 - 1 ML

₹ 6,884.70

In Stock

Quantity

1

Base Price: ₹ 6,884.70

GST (18%): ₹ 1,239.246

Total Price: ₹ 8,123.946

Quality Level

100

Assay

≥97.0% (GC/NT)

reaction suitability

reagent type: cross-linking reagent

refractive index

n20/D 1.454 (lit.)n20/D 1.459

bp

203 °C (lit.)

mp

22 °C (lit.)

density

0.998 g/mL at 20 °C (lit.)

functional group

Bocamine

SMILES string

NCCCNC(OC(C)(C)C)=O

InChI

1S/C8H18N2O2/c1-8(2,3)12-7(11)10-6-4-5-9/h4-6,9H2,1-3H3,(H,10,11)

Other Options

Image Product Name Manufacturer Price Range
50-176-2893
Sigma Aldrich Fine Chemicals Biosciences N-Boc-1,3-propanediamine >=97.0% (GC/NT) | 75178-96-0 | MFCD00210021 | 5ML
Sigma Aldrich Fine Chemicals Biosciences ₹ 45,381.02
50-176-2892
Sigma Aldrich Fine Chemicals Biosciences N-Boc-1,3-propanediamine >=97.0% (GC/NT) | 75178-96-0 | MFCD00210021 | 1ML
Sigma Aldrich Fine Chemicals Biosciences ₹ 29,452.32
50-242-9978
eMolecules​ Ambeed / tert-Butyl (3-aminopropyl)carbamate / 10g / 528568240 / A436098 / / 75178-96-0 / MFCD00210021 / 174.244 / C8H18N2O2
eMolecules​ ₹ 2,854.28
AR00361E
N-Boc-1,3-propanediamine
Aaron Chemicals LLC ₹ 342.24 - ₹ 44,148.96
CS-D0142
tert-Butyl (3-aminopropyl)carbamate
ChemScene ₹ 684.48 - ₹ 25,668.00
AB46694
75178-96-0 | N-Boc-1,3-diaminopropane
A2B Chem ₹ 427.80 - ₹ 15,400.80

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Description

  • Application: Tackling vancomycin-resistant bacteria with ′lipophilic–vancomycin–carbohydrate conjugates′: This study discusses the synthesis of derivatives using N-Boc-1,3-propanediamine to develop new antibacterial agents targeting resistant bacterial strains (Yarlagadda et al., 2015).Sulfonamides differing in the alkylamino substituent length–Synthesis, electrochemical characteristic, acid-base profile and complexation properties: The study involves N-Boc-1,3-propanediamine in the synthesis of novel sulfonamide derivatives with potential biochemical applications (Ciesielska et al., 2022).Direct α-alkylation of primary aliphatic amines enabled by CO2 and electrostatics: Research demonstrating selective α-alkylation of N-Boc-1,3-propanediamine, highlighting a novel method in organic synthesis (Ye et al., 2018).
  • Other Notes: Synthesis of spermidine analogues;[1] Preparation of pharmacologically active compounds.[2]

SAFETY INFORMATION

Pictograms

GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314

Precautionary Statements

P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Assay:
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reaction suitability:
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refractive index:
n20/D 1.454 (lit.)n20/D 1.459

bp:
203 °C (lit.)

mp:
22 °C (lit.)

density:
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functional group:
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SMILES string:
NCCCNC(OC(C)(C)C)=O

InChI:
1S/C8H18N2O2/c1-8(2,3)12-7(11)10-6-4-5-9/h4-6,9H2,1-3H3,(H,10,11)

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SMILES string:
COc1ccc(cc1)C(C)O

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