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1036260-43-1

(CIS)-3-Aminocyclobutanol, a cycloalkylamine, is an important chemical compound with the molecular formula C4H9NO. It is characterized by its geometric isomerism, featuring a "cis" configuration where two higher priority groups are on the same side of the chemical bond. (CIS)-3-AMINOCYCLOBUTANOL is typically found as a clear, colorless liquid and can be utilized in various chemical reactions as an intermediate. Its properties, such as boiling point, melting point, or specific optical rotation, may vary depending on factors like purity or temperature. Careful handling and adherence to safety guidelines are essential to prevent any hazardous impacts.

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  • 1036260-43-1 Structure

  • Basic information

    1. Product Name: (CIS)-3-AMINOCYCLOBUTANOL
    2. Synonyms: (CIS)-3-AMINOCYCLOBUTANOL;Cyclobutanol, 3-aMino-, cis-;(1s,3s)-3-aMinocyclobutanol
    3. CAS NO:1036260-43-1
    4. Molecular Formula: C4H9NO
    5. Molecular Weight: 87.12036
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036260-43-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 157.6 °C at 760 mmHg
    3. Flash Point: 49.1 °C
    4. Appearance: /
    5. Density: 1.153g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 15.00±0.40(Predicted)
    10. CAS DataBase Reference: (CIS)-3-AMINOCYCLOBUTANOL(CAS DataBase Reference)
    11. NIST Chemistry Reference: (CIS)-3-AMINOCYCLOBUTANOL(1036260-43-1)
    12. EPA Substance Registry System: (CIS)-3-AMINOCYCLOBUTANOL(1036260-43-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1036260-43-1(Hazardous Substances Data)

1036260-43-1 Usage

Uses

Used in Chemical Synthesis:
(CIS)-3-Aminocyclobutanol is used as a chemical intermediate for the synthesis of various compounds. Its unique "cis" configuration and cycloalkylamine structure make it a valuable building block in the preparation of complex molecules and pharmaceuticals.
Used in Pharmaceutical Industry:
(CIS)-3-Aminocyclobutanol is used as a key component in the development of new drugs. Its presence in chemical reactions can lead to the formation of novel molecules with potential therapeutic applications, contributing to the advancement of medicine.
Used in Research and Development:
(CIS)-3-Aminocyclobutanol is employed as a research compound in academic and industrial laboratories. Its unique properties and reactivity make it an interesting subject for studying chemical reactions, mechanisms, and the development of new synthetic methods.
Used in Material Science:
(CIS)-3-Aminocyclobutanol is used as a precursor in the synthesis of advanced materials, such as polymers and composites. Its incorporation into these materials can impart new properties, enhancing their performance in various applications, including electronics, coatings, and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 1036260-43-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,2,6 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1036260-43:
(9*1)+(8*0)+(7*3)+(6*6)+(5*2)+(4*6)+(3*0)+(2*4)+(1*3)=111
111 % 10 = 1
So 1036260-43-1 is a valid CAS Registry Number.

1036260-43-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (CIS)-3-AMINOCYCLOBUTANOL

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1036260-43-1 SDS

1036260-43-1Synthetic route

(1S,3S)-3-aminocyclobutan-1-ol
1036260-43-1

(1S,3S)-3-aminocyclobutan-1-ol

6-bromo-4-chloroquinoline-3-carboxylic acid ethyl ester
206257-39-8

6-bromo-4-chloroquinoline-3-carboxylic acid ethyl ester

ethyl 6-bromo-4-[(cis-3-hydroxycyclobutyl)amino]quinoline-3-carboxylate

ethyl 6-bromo-4-[(cis-3-hydroxycyclobutyl)amino]quinoline-3-carboxylate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl acetamide at 80 - 90℃; Inert atmosphere;93%
(1S,3S)-3-aminocyclobutan-1-ol
1036260-43-1

(1S,3S)-3-aminocyclobutan-1-ol

4-chloro-7-fluoro-6-(6-(methoxymethyl)pyridin-3-yl)quinoline-3-carboxamide

4-chloro-7-fluoro-6-(6-(methoxymethyl)pyridin-3-yl)quinoline-3-carboxamide

7-fluoro-4-((cis-3-hydroxycyclobutyl)amino)-6-(6-(methoxymethyl)pyridin-3-yl)quinoline-3-carboxamide

7-fluoro-4-((cis-3-hydroxycyclobutyl)amino)-6-(6-(methoxymethyl)pyridin-3-yl)quinoline-3-carboxamide

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl acetamide Inert atmosphere; Heating;72%
(1S,3S)-3-aminocyclobutan-1-ol
1036260-43-1

(1S,3S)-3-aminocyclobutan-1-ol

2-(5-amino-2-(furan-2-yl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-7-yl)-2-phenylpropanoic acid

2-(5-amino-2-(furan-2-yl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-7-yl)-2-phenylpropanoic acid

2-(5-amino-2-(furan-2-yl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-7-yl)-N-((1s,3s)-3-hydroxycyclobutyl)-2-phenylpropanamide

2-(5-amino-2-(furan-2-yl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-7-yl)-N-((1s,3s)-3-hydroxycyclobutyl)-2-phenylpropanamide

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; HATU In tetrahydrofuran at 20℃;44%
(1S,3S)-3-aminocyclobutan-1-ol
1036260-43-1

(1S,3S)-3-aminocyclobutan-1-ol

7-methoxyquinoline-3-carboxylic acid
474659-26-2

7-methoxyquinoline-3-carboxylic acid

N-((1s,3s)-3-hydroxycyclobutyl)-7-methoxyquinoline-3-carboxamide

N-((1s,3s)-3-hydroxycyclobutyl)-7-methoxyquinoline-3-carboxamide

Conditions
ConditionsYield
Stage #1: 7-methoxyquinoline-3-carboxylic acid With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 0.0833333h;
Stage #2: (1S,3S)-3-aminocyclobutan-1-ol In N,N-dimethyl-formamide		21%
(3R,3'R,4'S,6'S,8'R,8a'S)-6-chloro-8'-(3-chloro-2-fluorophenyl)-6'-neopentyl-3',4'-diphenyl 3',4',8',8a'-tetrahydrospiro[indoline-3,7'-pyrrolo[2,1-c][1,4]oxazine]-1',2(6'H)-dione
897365-81-0

(3R,3'R,4'S,6'S,8'R,8a'S)-6-chloro-8'-(3-chloro-2-fluorophenyl)-6'-neopentyl-3',4'-diphenyl 3',4',8',8a'-tetrahydrospiro[indoline-3,7'-pyrrolo[2,1-c][1,4]oxazine]-1',2(6'H)-dione

(1S,3S)-3-aminocyclobutan-1-ol
1036260-43-1

(1S,3S)-3-aminocyclobutan-1-ol

C41H42Cl2FN3O4
1443749-27-6

C41H42Cl2FN3O4

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 12h; Inert atmosphere;2.13 g

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