Cas 141120-76-5,3-Chloro-benzoic acid (1R,15S)-1-hydroxy-tricyclo[6.6.2.02,7]hexadeca-2(7),3,5,8(16)-tetraen-15-yl ester

141120-76-5

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Basic information

Product Name: 3-Chloro-benzoic acid (1R,15S)-1-hydroxy-tricyclo[6.6.2.0^2,7]hexadeca-2⁽⁷⁾,3,5,8⁽¹⁶⁾-tetraen-15-yl ester
Synonyms: 3-Chloro-benzoic acid (1R,15S)-1-hydroxy-tricyclo[6.6.2.0^2,7]hexadeca-2⁽⁷⁾,3,5,8⁽¹⁶⁾-tetraen-15-yl ester
CAS NO:141120-76-5
Molecular Formula:
Molecular Weight: 382.887
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: 3-Chloro-benzoic acid (1R,15S)-1-hydroxy-tricyclo[6.6.2.0^2,7]hexadeca-2⁽⁷⁾,3,5,8⁽¹⁶⁾-tetraen-15-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Chloro-benzoic acid (1R,15S)-1-hydroxy-tricyclo[6.6.2.0^2,7]hexadeca-2⁽⁷⁾,3,5,8⁽¹⁶⁾-tetraen-15-yl ester(141120-76-5)
EPA Substance Registry System: 3-Chloro-benzoic acid (1R,15S)-1-hydroxy-tricyclo[6.6.2.0^2,7]hexadeca-2⁽⁷⁾,3,5,8⁽¹⁶⁾-tetraen-15-yl ester(141120-76-5)

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: 141120-76-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141120-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,2 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141120-76:
(8*1)+(7*4)+(6*1)+(5*1)+(4*2)+(3*0)+(2*7)+(1*6)=75
75 % 10 = 5
So 141120-76-5 is a valid CAS Registry Number.

141120-76-5Upstream product

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141120-76-5Relevant academic research and scientific papers

Unusual reactivity of bent acenes: Reactions of [6](1,4)naphthalenophane and [6](1,4)anthracenophane with electrophiles

Tobe, Yoshito,Takemura, Akihiro,Jimbo, Mamoru,Takahashi, Tohru,Kobiro, Kazuya,Kakiuchi, Kiyomi

, p. 3479 - 3491 (1992)

The unusual reactivity of [6](1,4)naphthalenophane (2) and [6](1,4)anthracenophane (3), the smallest-bridged acenophanes hitherto known, in electrophilic reactions has been disclosed. These reactions include (i) acid-catalyzed telomerization, (ii) peracid

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