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S-(+)-1-[(4-(Dimethylamino)-3-methylphenyl)methyl]-5-(diphenylacetyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylic acid hydrate di(trifluoroacetate) salt is a complex organic compound with a unique molecular structure. It is a salt form of a carboxylic acid that includes a hydrous component and trifluoroacetate groups. S-(+)-1-[(4-(Dimethylamino)-3-methylphenyl)methyl]-5-(diphenylacetyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylic acid hydrate di(trifluoroacetate) salt has multiple functional groups, which contribute to its potential applications in various fields.

136676-91-0

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136676-91-0 Usage

Uses

Used in Pharmaceutical Research:
S-(+)-1-[(4-(Dimethylamino)-3-methylphenyl)methyl]-5-(diphenylacetyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylic acid hydrate di(trifluoroacetate) salt is used as a research compound for the development of new pharmaceuticals. Its complex structure and multiple functional groups make it a promising candidate for the design and synthesis of novel drugs with potential therapeutic effects.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, S-(+)-1-[(4-(Dimethylamino)-3-methylphenyl)methyl]-5-(diphenylacetyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylic acid hydrate di(trifluoroacetate) salt is utilized for studying its interactions with biological targets. Its unique molecular structure allows researchers to investigate its binding properties, selectivity, and potential therapeutic applications in treating various diseases and conditions.
Used in Drug Design and Development:
S-(+)-1-[(4-(Dimethylamino)-3-methylphenyl)methyl]-5-(diphenylacetyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylic acid hydrate di(trifluoroacetate) salt is employed as a key component in drug design and development processes. Its complex structure and functional groups can be modified and optimized to create new drug candidates with improved pharmacological properties, such as increased potency, selectivity, and reduced side effects.
Used in Chemical Synthesis:
In chemical synthesis, S-(+)-1-[(4-(Dimethylamino)-3-methylphenyl)methyl]-5-(diphenylacetyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylic acid hydrate di(trifluoroacetate) salt serves as a versatile building block for the synthesis of various organic compounds. Its unique structure and functional groups can be used to create new molecules with potential applications in different industries, such as materials science, agrochemicals, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 136676-91-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,6,7 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136676-91:
(8*1)+(7*3)+(6*6)+(5*6)+(4*7)+(3*6)+(2*9)+(1*1)=160
160 % 10 = 0
So 136676-91-0 is a valid CAS Registry Number.

136676-91-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name PD 123319 bistrifluoroacetate

1.2 Other means of identification

Product number -
Other names (S)-1-((4-(dimethylamino)-3-methylphenyl)methyl)-5-(diphenylacetyl)-4,5,6,7-tetrahydro-1H-imidazo(4,5-c)pyridine-6-carboxylic acid,difluoroacetate salt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:136676-91-0 SDS

136676-91-0Downstream Products

136676-91-0Relevant academic research and scientific papers

Synthesis and Structure-Activity Relationships of a Novel Series of Non-Peptide Angiotensin II Receptor Binding Inhibitors Specific for the AT2 Subtype

Blankley, C. John,Hodges, John C.,Klutchko, Sylvester R.,Himmelsbach, Richard J.,Chucholowski, Alexander,et al.

, p. 3248 - 3260 (2007/10/02)

Structure-activity relationships are reported for a novel class of 4,5,6,7-tetrahydro-1H-imidazopyridine-6-carboxylic acid derivatives that displace 125I-labeled angiotensin II from a specific subset of angiotensin II (Ang II) binding sites in rat

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