What is the 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride?

3-Amino-3-azabicyclo[3.3.0]octane hydrochloride is light yellow brown powder, while it's Molecular Formula is C7H14N2 . HCl. light yellow brown powder 3-Amino-3-azabicyclo[3,3,0]octane Hydrochloride is used as a reactant in the synthesis of cannabinoid receptor antagonists.

What is the CAS number for 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride?

The CAS number of 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride is 58108-05-7.

What is the 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride?

3-Amino-3-azabicyclo[3.3.0]octane hydrochloride is light yellow brown powder, while it's Molecular Formula is C7H14N2 . HCl. light yellow brown powder 3-Amino-3-azabicyclo[3,3,0]octane Hydrochloride is used as a reactant in the synthesis of cannabinoid receptor antagonists.

What is the CAS number for 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride?

The CAS number of 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride is 58108-05-7.

Reputable manufacturer supply 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride 58108-05-7 in stock with high standard

Q: What is 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride (58108-05-7) used for?

3-Amino-3-azabicyclo[3.3.0]octane hydrochloride, also known as N-amino-3-azabicyclo[3.3.0]octane monohydrochloride, is an organic compound with a unique bicyclic structure. It is a key intermediate in the synthesis of various pharmaceutical compounds, particularly those targeting the cannabinoid receptor.InChI:InChI=1/C7H14N2.ClH/c8-9-4-6-2-1-3-7(6)5-9;/h6-7H,1-5,8H2;1H

Product Details;

CasNo： 58108-05-7

Molecular Formula： C₇H₁₄N₂^.HCl

Appearance： light yellow brown powder

Reputable manufacturer supply 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride 58108-05-7 in stock with high standard

Molecular Formula:C7H14N2^.HCl
Molecular Weight:162.662
Appearance/Colour:light yellow brown powder
Melting Point:170-174 °C(lit.)
Boiling Point:229.9 °C at 760 mmHg
Flash Point:92.9 °C
PSA：29.26000
LogP:2.03220

3-Amino-3-azabicyclo[3.3.0]octane hydrochloride(Cas 58108-05-7) Usage

General Description	3-Amino-3-azabicyclo[3.3.0]octane hydrochloride is also referred to as N-amino-3-azabicyclo[3.3.0]octane monohydrochloride. Jilin Tianyun New Materials Co., Ltd. is a professional production enterprise that production, processing, and export, mainly engaged in various organic chemicals. We look forward to establishing a long-term stable and win-win business relationship with you.
Uses	3-Amino-3-azabicyclo[3.3.0]octane hydrochloride is used as a reactant in the synthesis of cannabinoid receptor antagonists. 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride is used as an intermediate in the synthesis of Gliclazide, which is used to treat type 2 diabetes.

InChI:InChI=1/C7H14N2.ClH/c8-9-4-6-2-1-3-7(6)5-9;/h6-7H,1-5,8H2;1H

58108-05-7 Relevant articles

Synthesis process of N-amino-3-azabicyclo [3, 3, 0] octane hydrochloride

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Paragraph 0017; 0027; 0030-0032; 0035-0037; 0040-0042; 0045-, (2021/05/29)

The invention provides a synthesis proce...

Method for preparing N-amino-3-aza-bicyclo [3, 3, 0] octane hydrochloride

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Paragraph 0030-0032, (2018/10/19)

The invention relates to a new method fo...

Applications of biological of Azo-Schiff base ligand and its metal complexes and: A review.

Ashoor, Lamia S.; Majeed, Rawa'a Abass; Al-Shemary, Rehab Kadhim Raheem

, AL-Muthanna Journal of Pure Science, 2021, Vol 8, Issue 1, p74

In 2016 Selma B[25], was prepared a novel azoSchiff base applying salicylaldehyde, aniline and 3-amino-3-azabicyclo[3.3.0]octane hydrochloride. The ligand were reacted with of Ni (II...

Influence of blood proteins on biomedical analysis. IX. Protective effects of human serum proteins on anion-induced degradation of gliclazide

Kobayashi,Igaki,Kimura,Sakoguchi,Shimosawa,Matsuoka

, p. 2957 - 2962 (2007/10/02)

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58108-05-7 Process route

: 1050666-51-7
N-amino-1,2-cyclopentanedicarboximide

: 58108-05-7
3-azabicyclo<3.3.0>oct-3-yl-amine monohydrochloride

Conditions

Conditions	Yield
N-amino-1,2-cyclopentanedicarboximide; With aluminum (III) chloride; In tetrahydrofuran; at 45 ℃; for 0.333333h; Large scale; With sodium tetrahydroborate; In tetrahydrofuran; for 6h; Reflux; Large scale; With hydrogenchloride; In tetrahydrofuran; pH=3; Solvent; Temperature; Large scale;	81.3%
Multi-step reaction with 2 steps 1: acetic acid; pyrographite; ruthenium(III) chloride trihydrate; hydrogen / water / 16 h / 140 °C / 60006 Torr / Autoclave 2: hydrogenchloride With hydrogenchloride; ruthenium(III) chloride trihydrate; hydrogen; pyrographite; acetic acid; In water;