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225185

Sigma-Aldrich

Cyclobutylamine

98%

Synonym(s):

Aminocyclobutane

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About This Item

Linear Formula:
C4H7NH2
CAS Number:
2516-34-9
Molecular Weight:
71.12
Beilstein:
2069297
EC Number:
219-736-0
MDL number:
MFCD00001328
UNSPSC Code:
12352100
PubChem Substance ID:
24853483
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.437 (lit.)

bp

81.5 °C/752 mmHg (lit.)

density

0.833 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

NC1CCC1

InChI

1S/C4H9N/c5-4-2-1-3-4/h4H,1-3,5H2

InChI key

KZZKOVLJUKWSKX-UHFFFAOYSA-N

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Related Categories

Pictograms

FlameCorrosion
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H225,H314

Hazard Classifications

Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

24.8 °F - closed cup

Flash Point(C)

-4 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM5933
MKCK3490
MKCF9135
MKCD9947
MKBX9526V

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T Maruyama et al.
Chemical & pharmaceutical bulletin, 38(10), 2719-2725 (1990-10-01)
9-Cyclobutyladenine (4a), cis- and trans-9-[3- (hydroxymethyl)cyclobutyl]adenine (4b) and 9-[3,3-bis(hydroxymethyl)cyclobutyl]adenine(4d) were prepared from the corresponding cyclobutylamine derivatives (1a, 1b and 1d). Guanine congeners (9a, cis- and trans-9b and 9d) and carbocyclic oxetanocin G (1',2'-trans-9f) were also prepared. Carbocyclic oxetanocin A(1',2'-trans-4f), the
McNaughton et al.
Journal of molecular spectroscopy, 196(2), 274-282 (1999-11-30)
The infrared spectrum of vinylamine, generated by pyrolysis of cyclobutylamine, has been investigated at low and high resolution. The rovibrational structure of the far infrared spectrum (0.002 cm(-1)) has been analyzed, and effective rotational and centrifugal distortion constants have been
Hartmut Schirok
The Journal of organic chemistry, 71(15), 5538-5545 (2006-07-15)
7-Azaindoles are versatile building blocks, especially in medicinal chemistry, where they serve as bioisosteres of indoles or purines. Herein, we are presenting a robust and flexible synthesis of 1,3- and 1,3,6-substituted 7-azaindoles starting from nicotinic acid derivatives or 2,6-dichloropyridine, respectively.

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