1006614-49-8 Usage
General Description
The chemical "(1R trans)-2-(3,4-difluorophenyl)cyclopropane amine. HCl" is a compound that consists of a cyclopropane ring with a 3,4-difluorophenyl group attached to it, as well as an amine functional group. The HCl in the name indicates that the compound is in its salt form, with a hydrogen chloride molecule attached. This chemical compound may have potential applications in the field of pharmaceuticals or organic synthesis, due to the unique structure and properties conferred by the cyclopropane and difluorophenyl groups. Further research and testing would be necessary to fully understand the potential uses and effects of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 1006614-49-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,6,1 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1006614-49:
(9*1)+(8*0)+(7*0)+(6*6)+(5*6)+(4*1)+(3*4)+(2*4)+(1*9)=108
108 % 10 = 8
So 1006614-49-8 is a valid CAS Registry Number.
1006614-49-8Relevant articles and documents
Preparation method of phenyl-containing compound
-
Paragraph 0099-0101, (2022/01/04)
The present invention discloses a method for preparing an phenyl-containing compound. The present invention provides a method for preparing a compound shown in formula I, comprising the following steps: in the presence of formamide or acetamide, in the pr
Preparation method of ticagrelor chiral intermediate
-
Paragraph 0031; 0052;0053, (2019/04/06)
The invention discloses a preparation method of a ticagrelor chiral intermediate. The ticagrelor chiral intermediate is trans-(1R, 2S)-2-(3, 4-difluorophenyl) cyclopropylamine. The method includes thesteps: taking cyclopropylamine as a raw material; perfo
Synthetic method of ticagrelor midbody
-
Paragraph 0017; 0018, (2017/10/13)
The invention provides a novel synthetic method of a ticagrelor midbody (1). The synthetic method comprises the following steps: enabling a compound (2) and a compound (3) to have asymmetric tertiary cyclization reaction under the catalysis of rhodium (a