Cas 891845-33-3,2-Thiophenecarboxylic acid, 5-amino-, cyclohexyl ester

891845-33-3

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Basic information

Product Name: 2-Thiophenecarboxylic acid, 5-amino-, cyclohexyl ester
Synonyms:
CAS NO:891845-33-3
Molecular Formula: C11H15NO2S
Molecular Weight: 225.312
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: 2-Thiophenecarboxylic acid, 5-amino-, cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Thiophenecarboxylic acid, 5-amino-, cyclohexyl ester(891845-33-3)
EPA Substance Registry System: 2-Thiophenecarboxylic acid, 5-amino-, cyclohexyl ester(891845-33-3)

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: 891845-33-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 891845-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,1,8,4 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 891845-33:
(8*8)+(7*9)+(6*1)+(5*8)+(4*4)+(3*5)+(2*3)+(1*3)=213
213 % 10 = 3
So 891845-33-3 is a valid CAS Registry Number.

891845-33-3Upstream product

891845-32-2 cyclohexyl 5-nitro-2-thiophenecarboxylate

891845-33-3Downstream Products

891844-72-7 N-[({5-[(cyclohexyloxy)carbonyl]-2-thienyl}amino)carbonyl]-N-{[2-methyl-7-(2-naphthalenylmethyl)imidazo[2,1-b][1,3]thiazol-7-ium-6-yl]methyl}-L-tyrosinamide trifluoroacetate

891845-33-3Relevant academic research and scientific papers

Muscarinic acetylcholine receptor antagonists: SAR and optimization of tyrosine ureas

Jin, Jian,Wang, Yonghui,Shi, Dongchuan,Wang, Feng,Fu, Wei,Davis, Roderick S.,Jin, Qi,Foley, James J.,Sarau, Henry M.,Morrow, Dwight M.,Moore, Michael L.,Rivero, Ralph A.,Palovich, Michael,Salmon, Michael,Belmonte, Kristen E.,Busch-Petersen, Jakob

, p. 5481 - 5486 (2008)

SAR exploration of multiple regions of a tyrosine urea template led to the identification of very potent muscarinic acetylcholine receptor antagonists such as 10b with good subtype selectivity for M3 over M1. The structure-activity r

Discovery of novel and long acting muscarinic acetylcholine receptor antagonists

Jin, Jian,Wang, Yonghui,Shi, Dongchuan,Wang, Feng,Davis, Roderick S.,Jin, Qi,Fu, Wei,Foley, James J.,Webb, Edward F.,Dehaas, Chris J.,Berlanga, Manuela,Burman, Miriam,Sarau, Henry M.,Morrow, Dwight M.,Rao, Parvathi,Kallal, Lorena A.,Moore, Michael L.,Rivero, Ralph A.,Palovich, Michael,Salmon, Michael,Belmonte, Kristen E.,Busch-Petersen, Jakob

supporting information; experimental part, p. 4866 - 4869 (2009/08/09)

High throughput screening and subsequent optimization led to the discovery of novel quaternary ammonium salts as highly potent muscarinic acetylcholine receptor antagonists with excellent selectivity. Compounds 8a, 13a, and 13b showed excellent inhibitory

NOVEL M3 MUSCARINIC ACETYCHOLINE RECEPTOR ANTAGONISTS

-

Page/Page column 56, (2008/06/13)

Muscarinic Acetylcholine receptor antagonists and methods of using them are provided.

QUATERNARY AMMONIUM SALTS OF FUSED HETEAROMATIC AMINES AS NOVEL MUSCARINIC ACETYLCHOLINE RECEPTOR ANTAGONISTS

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Page/Page column 15, (2010/11/08)

Novel derivatives of cyclic amines, pharmaceutical compositions, processes for their preparation, and use thereof in treating muscarinic acetylcholine receptor mediated diseases are provided.

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