Cas 97847-89-7,(1,1-dimethyl-5-phenyl-pentyl)-amine hydrochloride

97847-89-7

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Basic information

Product Name: (1,1-dimethyl-5-phenyl-pentyl)-amine hydrochloride
Synonyms: (1,1-dimethyl-5-phenyl-pentyl)-amine hydrochloride
CAS NO:97847-89-7
Molecular Formula:
Molecular Weight: 227.777
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1,1-dimethyl-5-phenyl-pentyl)-amine hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: (1,1-dimethyl-5-phenyl-pentyl)-amine hydrochloride(97847-89-7)
EPA Substance Registry System: (1,1-dimethyl-5-phenyl-pentyl)-amine hydrochloride(97847-89-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 97847-89-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 97847-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,4 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 97847-89:
(7*9)+(6*7)+(5*8)+(4*4)+(3*7)+(2*8)+(1*9)=207
207 % 10 = 7
So 97847-89-7 is a valid CAS Registry Number.

97847-89-7Upstream product

97847-89-7Downstream Products

97847-89-7Relevant academic research and scientific papers

Palladium-Catalyzed Arylation of Unactivated γ-Methylene C(sp3)-H and δ-C-H Bonds with an Oxazoline-Carboxylate Auxiliary

Ling, Peng-Xiang,Fang, Sheng-Long,Yin, Xue-Song,Chen, Kai,Sun, Bo-Zheng,Shi, Bing-Feng

supporting information, p. 17503 - 17507 (2016/01/25)

A palladium-catalyzed arylation of unactivated γ-methylene C(sp3)-H and remote δ-C-H bonds by using an oxazoline-carboxylate directing group has been developed. Arylation occurs with a broad substrate scope and high tolerance of functional groups (i.e., halogen, nitro, cyano, ether, trifluoromethyl, amine, and ester). The oxazoline-type auxiliary can be removed under acidic conditions.

SUBSTITUTED BENZOXAZOLONE DERIVATIVES AS ACID CERAMIDASE INHIBITORS, AND THEIR USE AS MEDICAMENTS

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Paragraph 20; 39; 48, (2015/12/31)

The present invention relates to substituted benzoxazolone derivatives as acid ceramidase inhibitors, pharmaceutical compositions containing these inhibitors and methods of inhibiting acid ceramidase for the treatment of disorders in which modulation of the levels of ceramide is clinically relevant. The invention also provides substituted benzoxazolone derivatives for use in the treatment of cancer, inflammation, pain, inflammatory pain or pulmonary diseases.

1-DIPHENYLPHOSPHINYL-2,2-DIMETHYLAZIRIDINE - A NEW PRECURSOR OF α,α-DIMETHYLARYLALKYLAMINES

Buchowiecki, Wieslaw,Grosman-Zjawiona, Zofia,Zjawiony, Jordan

, p. 1245 - 1248 (2007/10/02)

The new synthesis of α,α-dimethylarylalkylamines from 1-diphenylphosphinyl-2,2-dimethylaziridine is described.

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