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[(Diphenylmethyl)sulfanyl]methanimidamide hydrobromide is an organosulfur compound that is a hydrobromide salt form of a compound used in organic synthesis and pharmaceutical research. It is a crystalline solid with a molecular formula of C14H16BrN3S and a molar mass of 328.263 g/mol. Known for its potent biological activities, [(Diphenylmethyl)sulfanyl]methanimidamide hydrobromide may have potential applications in the development of new drugs and pharmaceuticals, although further research is needed to fully understand its potential uses.

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  • 90280-15-2 Structure
  • Basic information

    1. Product Name: [(Diphenylmethyl)sulfanyl]methanimidamide hydrobromide
    2. Synonyms: [(Diphenylmethyl)sulfanyl]methanimidamide hydrobromide;2-BENZHYDRYL-2-THIOPSEUDOUREA HYDROBROMIDE;[(Diphenylmethyl)sulfanyl]methanimidamide hydrochloride
    3. CAS NO:90280-15-2
    4. Molecular Formula: BrH*C14H14N2S
    5. Molecular Weight: 323
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90280-15-2.mol
  • Chemical Properties

    1. Melting Point: 180-182 °C(Solv: ethanol (64-17-5); ethyl ether (60-29-7))
    2. Boiling Point: 377.8°Cat760mmHg
    3. Flash Point: 182.3°C
    4. Appearance: /
    5. Density: 1.15g/cm3
    6. Vapor Pressure: 6.56E-06mmHg at 25°C
    7. Refractive Index: 1.621
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: [(Diphenylmethyl)sulfanyl]methanimidamide hydrobromide(CAS DataBase Reference)
    11. NIST Chemistry Reference: [(Diphenylmethyl)sulfanyl]methanimidamide hydrobromide(90280-15-2)
    12. EPA Substance Registry System: [(Diphenylmethyl)sulfanyl]methanimidamide hydrobromide(90280-15-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 90280-15-2(Hazardous Substances Data)

90280-15-2 Usage

Uses

Used in Pharmaceutical Research:
[(Diphenylmethyl)sulfanyl]methanimidamide hydrobromide is used as a reagent in the formation of various compounds for pharmaceutical research, due to its potent biological activities and potential applications in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, [(Diphenylmethyl)sulfanyl]methanimidamide hydrobromide is used as a reagent to facilitate the synthesis of a range of organic compounds, leveraging its unique chemical properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 90280-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,8 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90280-15:
(7*9)+(6*0)+(5*2)+(4*8)+(3*0)+(2*1)+(1*5)=112
112 % 10 = 2
So 90280-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N2S/c15-14(16)17-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13H,(H3,15,16)

90280-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name benzhydryl carbamimidothioate

1.2 Other means of identification

Product number -
Other names benzhydrylthiocarboxamidine hydrochloride

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:90280-15-2 SDS

90280-15-2Relevant articles and documents

A daily single dose of a novel modafinil analogue CE-123 improves memory acquisition and memory retrieval

Kristofova, Martina,Aher, Yogesh D.,Ilic, Marija,Radoman, Bojana,Kalaba, Predrag,Dragacevic, Vladimir,Aher, Nilima Y.,Leban, Johann,Korz, Volker,Zanon, Lisa,Neuhaus, Winfried,Wieder, Marcus,Langer, Thierry,Urban, Ernst,Sitte, Harald H.,Hoeger, Harald,Lubec, Gert,Aradska, Jana

, p. 83 - 94 (2018)

Dopamine reuptake inhibitors have been shown to improve cognitive parameters in various tasks and animal models. We recently reported a series of modafinil analogues, of which the most promising, 5-((benzhydrylsulfinyl)methyl) thiazole (CE-123), was selec

A novel heterocyclic compound targeting the dopamine transporter improves performance in the radial arm maze and modulates dopamine receptors D1-D3

Saroja, Sivaprakasam R.,Aher, Yogesh D.,Kalaba, Predrag,Aher, Nilima Y.,Zehl, Martin,Korz, Volker,Subramaniyan, Saraswathi,Miklosi, Andras G.,Zanon, Lisa,Neuhaus, Winfried,H?ger, Harald,Langer, Thierry,Urban, Ernst,Leban, Johann,Lubec, Gert

, p. 127 - 137 (2016)

A series of compounds targeting the dopamine transporter (DAT) haS been shown to improve memory performance most probably by re-uptake inhibition. Although specific DAT inhibitors are available, there is limited information about specificity, mechanism an

Heterocyclic Analogues of Modafinil as Novel, Atypical Dopamine Transporter Inhibitors

Kalaba, Predrag,Aher, Nilima Y.,Ili?, Marija,Draga?evi?, Vladimir,Wieder, Marcus,Miklosi, Andras G.,Zehl, Martin,Wackerlig, Judith,Roller, Alexander,Beryozkina, Tetyana,Radoman, Bojana,Saroja, Sivaprakasam R.,Lindner, Wolfgang,Gonzalez, Eduardo Perez,Bakulev, Vasiliy,Leban, Johann Jakob,Sitte, Harald H.,Urban, Ernst,Langer, Thierry,Lubec, Gert

, p. 9330 - 9348 (2017)

Modafinil is a wake promoting compound with high potential for cognitive enhancement. It is targeting the dopamine transporter (DAT) with moderate selectivity, thereby leading to reuptake inhibition and increased dopamine levels in the synaptic cleft. A s

Structure-Activity Relationships of Novel Thiazole-Based Modafinil Analogues Acting at Monoamine Transporters

Kalaba, Predrag,Ili?, Marija,Aher, Nilima Y.,Draga?evi?, Vladimir,Wieder, Marcus,Zehl, Martin,Wackerlig, Judith,Beyl, Stanislav,Sartori, Simone B.,Ebner, Karl,Roller, Alexander,Lukic, Natalie,Beryozkina, Tetyana,Gonzalez, Eduardo Rene Perez,Neill, Philip,Khan, Jawad Akbar,Bakulev, Vasiliy,Leban, Johann Jakob,Hering, Steffen,Pifl, Christian,Singewald, Nicolas,Lubec, Jana,Urban, Ernst,Sitte, Harald H.,Langer, Thierry,Lubec, Gert

supporting information, p. 391 - 417 (2020/02/20)

Atypical dopamine reuptake inhibitors, such as modafinil, are used for the treatment of sleeping disorders and investigated as potential therapeutics against cocaine addiction and for cognitive enhancement. Our continuous effort to find modafinil analogue

A novel heterocyclic compound improves working memory in the radial arm maze and modulates the dopamine receptor D1R in frontal cortex of the Sprague-Dawley rat

Hussein, Ahmed M.,Aher, Yogesh D.,Kalaba, Predrag,Aher, Nilima Y.,Draga?evi?, Vladimir,Radoman, Bojana,Ili?, Marija,Leban, Johann,Beryozkina, Tetyana,Ahmed, Abdel Baset M.A.,Urban, Ernst,Langer, Thierry,Lubec, Gert

, p. 308 - 315 (2017/06/27)

A series of compounds have been shown to enhance cognitive function via the dopaminergic system and indeed the search for more active and less toxic compounds is continuing. It was therefore the aim of the study to synthetise and test a novel heterocyclic

HETEROCYCLIC COMPOUNDS WITH WORKING MEMORY ENHANCING ACTIVITY

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Page/Page column 37; 41, (2016/02/29)

The present invention relates to a chemical compound having the general formula (I): wherein R1 and R2 are, equal or independently, aryl, heteroaryl; wherein RTA is a 2-1,3-, or 4- 1,3- or 5-1,3-thiazole ring and its use in for improving; the short term memory and/or the working memory.

IMPROVED PROCESS FOR PREPARING BENZHYDRYLTHIOACETAMIDE

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Page/Page column 9-10, (2008/06/13)

The present invention is directed to an improved process for preparing modafinil wherein benzhydrylthioacetate is prepared in high yield and purity by the reaction of a haloacetate with the reaction product of thiourea and benzhydrol. The reaction employing the haloacetate is conducted in a solvent comprising an organic solvent such as methanol having dissolved therein an organic base or an inorganic basic salt such as sodium bicarbonate. The resulting benzhydrylthioacetate can be amidated and then oxidized to provide the pharmaceutical grade modafinil in high yield and purity.

PREPARATIONS OF A SULFINYL ACETAMIDE

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Page 12, (2008/06/13)

The present invention provides processes for the preparation of modafinil which includes the step of reacting benzhydrylthiol and chloroacetamide.

Process for the preparation of diphenylmethylthioacetamide

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Referential example 1, (2010/01/31)

The invention provides a process for the preparation of diphenylmethylthioacetamide (I) as described in Scheme 4 comprising reacting of the isothiouronium salt or its corresponding base of the formula IV with an acetamide of the formula XCH2CONH2, wherein X represents a halogen, M represents an alkali metal and A represents an anion, in a protic medium at a temperature of less than 100° C.

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