151860-17-2

• 

• Basic information

  1. Product Name: 6-Amino-3-benzyl-3-azabicyclo[3.1.0]hexane
  2. Synonyms: 6-Amino-3-benzyl-3-azabicyclo[3.1.0]hexane;3-Benzyl-3-aza-bicyclo[3.1.0]hex-6-ylamine;3-(3-Methylphenyl)bicyclo[3.1.0]hexan-6-aMine;(1R,5S,6s)-3-Benzyl-3-azabicyclo[3.1.0]hexan-6-aMine
  3. CAS NO:151860-17-2
  4. Molecular Formula: C₁₂H₁₆N₂
  5. Molecular Weight: 188.27
  6. EINECS: N/A
  7. Product Categories: pharmacetical
  8. Mol File: 151860-17-2.mol
  9. Article Data: 9

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 280.2 °C at 760 mmHg
  3. Flash Point: 111.5 °C
  4. Appearance: /
  5. Density: 1.145 g/cm³
  6. Vapor Pressure: 0.004mmHg at 25°C
  7. Refractive Index: 1.615
  8. Storage Temp.: 2-8°C
  9. Solubility: N/A
  10. CAS DataBase Reference: 6-Amino-3-benzyl-3-azabicyclo[3.1.0]hexane(CAS DataBase Reference)
  11. NIST Chemistry Reference: 6-Amino-3-benzyl-3-azabicyclo[3.1.0]hexane(151860-17-2)
  12. EPA Substance Registry System: 6-Amino-3-benzyl-3-azabicyclo[3.1.0]hexane(151860-17-2)

• 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: 151860-17-2(Hazardous Substances Data)

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• 3-Azabicyclo[3.1.0]hexan-6-amine, 3-(phenylmethyl)-, (1α,5α,6α)-

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• 3-Azabicyclo[3.1.0]hexan-6-amine, 3-(phenylmethyl)-, (1α,5α,6α)-

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• 6-Amino-3-benzyl-3-azabicyclo[3.1.0]hexane

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• 3-Azabicyclo[3.1.0]hexan-6-amine, 3-(phenylmethyl)-, (1α,5α,6α)-

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• 3-Azabicyclo[3.1.0]hexan-6-amine, 3-(phenylmethyl)-, (1α,5α,6α)- cas 151860-17-2

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• 6-Amino-3-benzyl-3-azabicyclo[3.1.0]hexane

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• 3-Azabicyclo[3.1.0]hexan-6-amine, 3-(phenylmethyl)-, (1α,5α,6α)- CAS NO.151860-17-2

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• 3-BENZYL-3-AZA-BICYCLO[3.1.0]HEX-6-YLAMINE

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• 6-Amino-3-benzyl-3-azabicyclo[3.1.0]hexane

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151860-17-2 Usage

General Description

6-Amino-3-benzyl-3-azabicyclo[3.1.0]hexane is a complex, organic chemical compound belonging to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene. Its molecule is characterized by a structure that includes an azabicyclohexane ring, which is a skeleton with two additional ring junctions, and a benzyl group, a type of organic substitution in which a hydrogen atom in benzene is replaced by a substituent. Information regarding its specific uses, properties or potential industrial applications is not widely available in published literature, indicating that it might be primarily used or studied in advanced chemical research. It's crucial to handle it carefully as its health effects aren't well-documented as well.

Check Digit Verification of cas no

The CAS Registry Mumber 151860-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,8,6 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 151860-17:
(8*1)+(7*5)+(6*1)+(5*8)+(4*6)+(3*0)+(2*1)+(1*7)=122
122 % 10 = 2
So 151860-17-2 is a valid CAS Registry Number.

InChI:InChI=1/C12H16N2/c13-12-10-7-14(8-11(10)12)6-9-4-2-1-3-5-9/h1-5,10-12H,6-8,13H2

151860-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	3-benzyl-3-aza-bicyclo[3.1.0]hexan-6-amine

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:151860-17-2 SDS

151860-17-2Upstream product

• 232598-24-2 (1α, 5α, 6α)-6-Acetamido-3-benzyl-3-azabicyclo[3.1.0]hexane 
• 151860-15-0 (1α,5α,6α)-3-N-benzyl-6-nitro-2,4-dioxo-3-azabicyclo[3.1.0]hexane 
• 1631-26-1 1-benzyl-1H-pyrrole-2,5-dione 
• 151860-16-1 (1α,5α,6α)-3-N-benzyl-6-nitro-3-azabicyclo[3.1.0]hexane 

151860-17-2Downstream Products

• 185693-08-7 (1α,5α,6α)-6-amino-3-azabicyclo[3.1.0]hexane 
• 845626-36-0 3-benzyl-N,N-dimethyl-3-azabicyclo[3.1.0]hexan-6-amine 
• 858342-02-6 C₁₅H₂₀N₂O₂ 
• 845626-26-8 C₁₈H₂₈N₂O₂Si 
• 712355-73-2 (1α, 5α, 6α)-6-N-(3-azabicyclo [3.1. 0] hexyl-3-benzyl)-2-cyclohexyl-2-hydroxy-2-phenyl acetamide 
• 712356-53-1 (1α, 5α, 6α)-6N-(3-azabicyclo [3.1.0] hexyl-3-benzyl)-2-chloro acetamide 
• 134575-66-9 7-([1α,5α,6α]-6-tert-Butoxycarbonylamino-3-azabicyclo[3.1.0]hex-3-yl)-6-fluoro-1-(2,4-difluorophenyl)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid,ethyl ester 
• 256369-34-3 (1α,5α,6α)-6-Amino-3-azabicyclo[3.1.0]hexane ditosylate salt 
• 146836-84-2 trovafloxacin mesylate 
• 134575-17-0 tert-butyl (1R,5S,6R)-3-azabicyclo[3.1.0]hexan-6-ylcarbamate 

151860-17-2Relevant articles and documents

Synthesis of azabicyclo[3.1.0]amine analogues of anacardic acid as potent antibacterial agents

Vempati, Ravi Kumar,Reddy,Alapati, Srinivasa Rao,Dubey

, p. 986 - 994 (2013/06/26)

Azabicyclo[3.1.0]amine analogues of anacardic acid (16a, 16b, 18a, 18b, 19 and 19b) were synthesized from anacardic acid and tested for their antibacterial activity against Gram positive and Gram negative bacteria. Most of the compounds are having potency at par with ampicillin and inferior with other standard drugs.

Discovery of conformationally rigid 3-azabicyclo[3.1.0]hexane-derived dipeptidyl peptidase-IV inhibitors

Sattigeri, Jitendra A.,Andappan, Murugaiah M.S.,Kishore, Kaushal,Thangathirupathy, Srinivasan,Sundaram, Sinduja,Singh, Shuchita,Sharma, Suchitra,Davis, Joseph A.,Chugh, Anita,Bansal, Vinay S.

scheme or table, p. 4087 - 4091 (2009/04/10)

The induction of conformationally restricted N-(aryl or heteroaryl)-3-azabicyclo[3.1.0]hexane derivatives at P2 region of compounds of 2-cyanopyrrolidine class was explored to develop novel DPP-IV inhibitors. The synthesis, structure-activity r

SUBSTITUTED AZABICYCLO HEXANE DERIVATIVES AS MUSCARINIC RECEPTOR ANTAGONISTS

-

Page 18, (2008/06/13)

The present invention relates to a radio telephony network (1) supporting at least one link of a radio channel (6) for a packet data transmission service. The radio telephony network (1) comprises a plurality of network controllers (RNC). Each network con

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