Cas 1190368-98-9,(S,S)-2,2'''-dicyclohexyloxy-2'.2''-dimethyl-1,1':3',3'':1'',1'''-quarternaphthalene

1190368-98-9

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Basic information

Product Name: (S,S)-2,2'''-dicyclohexyloxy-2'.2''-dimethyl-1,1':3',3'':1'',1'''-quarternaphthalene
Synonyms:
CAS NO:1190368-98-9
Molecular Formula:
Molecular Weight: 730.99
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: (S,S)-2,2'''-dicyclohexyloxy-2'.2''-dimethyl-1,1':3',3'':1'',1'''-quarternaphthalene(CAS DataBase Reference)
NIST Chemistry Reference: (S,S)-2,2'''-dicyclohexyloxy-2'.2''-dimethyl-1,1':3',3'':1'',1'''-quarternaphthalene(1190368-98-9)
EPA Substance Registry System: (S,S)-2,2'''-dicyclohexyloxy-2'.2''-dimethyl-1,1':3',3'':1'',1'''-quarternaphthalene(1190368-98-9)

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: 1190368-98-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1190368-98-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,3,6 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1190368-98:
(9*1)+(8*1)+(7*9)+(6*0)+(5*3)+(4*6)+(3*8)+(2*9)+(1*8)=169
169 % 10 = 9
So 1190368-98-9 is a valid CAS Registry Number.

1190368-98-9Upstream product

75-16-1 methylmagnesium bromide

1190368-98-9Downstream Products

1190368-99-0 (S,S)-2',2''-dibromomethyl-2,2'''-dicyclohexyloxy-1,1':3',3'':1'',1'''-quarternaphthalene

1190368-98-9Relevant academic research and scientific papers

The practical synthesis of double axial chiral guanidines

Guo, Qun-Sheng,Du, Da-Ming

, p. 197 - 202 (2009)

Two novel double axial chiral guanidines were designed according to the concept of double axial chirality. The practical synthetic procedures from (S)-1, 1'-binaphthol have been developed. The title compounds were fully characterized by NMR, MS, IR and el

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