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(1R trans)-2-(3,4-difluorophenyl)cyclopropane amine is an organic compound characterized by its cyclopropane ring and difluorophenyl group. It is a chiral molecule with a specific configuration, which is important for its reactivity and potential applications.

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  • 1156491-10-9 Structure
  • Basic information

    1. Product Name: (1R trans)-2-(3,4-difluorophenyl)cyclopropane amine
    2. Synonyms: (1R,2S)-2-(3,4-difluorophenyl)cyclopropanaMine Hydrochloride(1:1);(1R,2S)-2-(3,4-Difluorophenyl)-cyclopropan-1-aMine HCL;(1R trans)-2-(3,4-difluorophenyl)cyclopropane aMine hydrochloride;(1R,2S)-rel-2-(3,4-Difluorophenyl)cyclopropanami;2-(3,4-Difluoro-phenyl)-cyclopropylamine;(1R trans)-2-(3,4-difluorophenyl)cyclopropane amine;(1R,2S)-rel-2-(3,4-Difluorophenyl)cyclopropanamine hydrochloride;CYCLOPROPANAMINE, 2-(3,4-DIFLUOROPHENYL)-, HYDROCHLORIDE (1:1), (1R,2S)-REL-
    3. CAS NO:1156491-10-9
    4. Molecular Formula: C9H10ClF2N
    5. Molecular Weight: 205.6322064
    6. EINECS: 1308068-626-2
    7. Product Categories: Intermediate of Ticagrelor
    8. Mol File: 1156491-10-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
    8. Solubility: DMSO (Slightly), Methanol (Slightly)
    9. CAS DataBase Reference: (1R trans)-2-(3,4-difluorophenyl)cyclopropane amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R trans)-2-(3,4-difluorophenyl)cyclopropane amine(1156491-10-9)
    11. EPA Substance Registry System: (1R trans)-2-(3,4-difluorophenyl)cyclopropane amine(1156491-10-9)
  • 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: 1156491-10-9(Hazardous Substances Data)

1156491-10-9 Usage

Uses

Used in Pharmaceutical Industry:
(1R trans)-2-(3,4-difluorophenyl)cyclopropane amine is used as an intermediate in the synthesis of ticagrelor (T437700), a medication used to prevent blood clots in patients with acute coronary syndrome or a history of heart attack.
The compound's specific configuration and reactivity make it a valuable building block in the development of pharmaceuticals, particularly those targeting cardiovascular conditions. Its use in the synthesis of ticagrelor highlights its importance in the creation of life-saving medications.

Check Digit Verification of cas no

The CAS Registry Mumber 1156491-10-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,6,4,9 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1156491-10:
(9*1)+(8*1)+(7*5)+(6*6)+(5*4)+(4*9)+(3*1)+(2*1)+(1*0)=149
149 % 10 = 9
So 1156491-10-9 is a valid CAS Registry Number.
InChI:InChI=1S/C9H9F2N.ClH/c10-7-2-1-5(3-8(7)11)6-4-9(6)12;/h1-3,6,9H,4,12H2;1H/t6?,9-;/m1./s1

1156491-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S)-2-(3,4-difluorophenyl)cyclopropanamine hydrochloride

1.2 Other means of identification

Product number -
Other names (1R,2S)-rel-2-(3,4-Difluorophenyl)cyclopropanamine hydrochloride

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:1156491-10-9 SDS

1156491-10-9Relevant articles and documents

Preparation method of chiral aromatic cyclopropylamine and salt thereof and intermediate used in preparation method

-

, (2020/06/20)

The embodiment of the invention provides a preparation method of a compound as shown in a formula I or salt thereof, which comprises the following steps: (1) reacting a compound as shown in a formulaVI with a compound as shown in a formula VII in a first

Preparation method of ticagrelor

-

, (2018/04/21)

The invention discloses a preparation method of ticagrelor. The preparation method comprises the following steps: (1) preparation of ticagrelor intermediate product 1-TK acid; (2) preparation of ticagrelor intermediate product 2-TK-amide; (3) preparation of ticagrelor intermediate product 3-TK-amino compound hydrochloride; (4) preparation of ticagrelor intermediate product 4-TK-amino compound R-tartrate; ( 5) preparation of ticagrelor intermediate product 5-TK-amino compound L-mandelate; and (6) preparation of ticagrelor-TK. The preparation method has the advantages of cost advantage, mature and stable process, stable product quality, and safe and reliable production process.

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