6685-76-3

Basic information

• Product Name: PHENYLGUANIDINE HYDROGEN CARBONATE
• Synonyms: PHENYLGUANIDINE HYDROGEN CARBONATE;N-PHENYL GUANIDINE CARBONATE;carbonic acid, compound with phenylguanidine (1:1);Phenylguanidine bicarbonate;Phenylguanidine carbonate
• CAS NO: 6685-76-3
• Molecular Formula: CH₂O₃*C₇H₉N₃
• Molecular Weight: 197.19
• EINECS: 229-729-4
• Mol File: 6685-76-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: 149-153 °C(lit.)
• Boiling Point: 428.8 °C at 760 mmHg
• Flash Point: 213.1 °C
• Appearance: /
• CAS DataBase Reference: PHENYLGUANIDINE HYDROGEN CARBONATE(CAS DataBase Reference)
• NIST Chemistry Reference: PHENYLGUANIDINE HYDROGEN CARBONATE(6685-76-3)
• EPA Substance Registry System: PHENYLGUANIDINE HYDROGEN CARBONATE(6685-76-3)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 6685-76-3(Hazardous Substances Data)

Usage

General Description

Phenylguanidine hydrogen carbonate is a chemical compound that is commonly used as a reagent in organic synthesis. It is a white crystalline solid that is soluble in water and has a faint ammonia-like odor. PHENYLGUANIDINE HYDROGEN CARBONATE is often utilized in the production of various pharmaceuticals and dyes. It is also employed as a catalyst in the synthesis of certain organic compounds. Additionally, phenylguanidine hydrogen carbonate is known for its ability to act as a corrosion inhibitor in certain industrial processes. Overall, this chemical is widely used in the field of organic chemistry for its versatile properties and applications.

Upstream product

• 420-04-2 CYANAMID 
• 497-19-8 sodium carbonate 
• 62-53-3 aniline 
• 129226-13-7 4-Phenyl-5-[(E)-propylimino]-4,5-dihydro-[1,2,4]thiadiazol-3-ylamine 
• 13140-47-1 N-n-propyl-N'-phenylthiourea 

Downstream Products

• 930581-48-9 {4-[2-(phenyl(methyl)amino)-4-methylthiazol-5-yl]pyrimidin-2-yl}-N-phenylamine 
• 1333391-33-5 {4-[2-(o-tolyl(methyl)amino)-4-methylthiazol-5-yl]pyrimidin-2-yl}-N-phenylamine 
• 1333391-28-8 {4-[2-(m-tolyl(methyl)amino)-4-methylthiazol-5-yl]pyrimidin-2-yl}-N-phenylamine 
• 1333391-22-2 {4-[2-(p-tolyl(methyl)amino)-4-methylthiazol-5-yl]pyrimidin-2-yl}-N-phenylamine 
• 1333391-47-1 (4-{2-[(2-chlorophenyl)(methyl)amino]-4-methylthiazol-5-yl}pyrimidin-2-yl)-N-phenylamine 
• 1333391-23-3 (4-{2-[(4-chlorophenyl)(methyl)amino]-4-methylthiazol-5-yl}pyrimidin-2-yl)-N-phenylamine 
• 1333391-35-7 (4-{2-[(3,4-dichlorophenyl)(methyl)amino]-4-methylthiazol-5-yl}pyrimidin-2-yl)-N-phenylamine 
• 1333391-37-9 (4-{2-[(3-chloro-4-fluorophenyl)(methyl)amino]-4-methylthiazol-5-yl}pyrimidin-2-yl)-N-phenylamine 
• 31793-65-4 phenyl-quinazolin-2-yl-amine 
• 796857-67-5 2-anilino-4-(1-isopropyl-2-formylimidazol-5-yl)pyrimidine 
• 50427-08-2 6-methyl-2-phenylaminopyrimidin-4(3H)-one 

Relevant articles and documents

Method for preparing mepanipyrim

The invention provides a preparation method of mepanipyrim and belongs to the field of pesticide chemical synthesis technologies. The preparation method of the mepanipyrim comprises the following steps: firstly, reacting phenyl guanidine salt with ethyl acetoacetate so as to prepare phenylamino pyrimidone, reacting the phenylamino pyrimidone with phosphorus oxychloride so as to prepare 2-chloro-pyrimidine phenylamine; subsequently, carrying out coupling and crossing reaction between the 2-chloro-pyrimidine phenylamine and alkyne so as to prepare mepanipyrim. The preparation method of mepanipyrim has the advantages that the used raw materials and reagents are cheap and easily available; the reaction process is simple, the reaction conditions are mild, the cost is low, the yield is high, a good condition is created for industrial large-scale production and commercialization of the products.

Substituted benzene derivatives useful as neuraminidase inhibitors

A compound of the Formula (I): STR1 or pharmaceutically-suitable salts or prodrug forms thereof, wherein: n is 0-1; m is 0; p is 0-1; R1 is --CO2 H; R2 is selected from the group consisting of H, --OH, and --NH2 ; R3 is H; R4 is --C(O)NHR8 ; R5 is --NHC(R6)NH2 R6 is selected from the group consisting of =NH, =NOH, =NCN, =O, and =S; and R8 is selected from the group consisting of C1 -C4 linear or branched alkyl substituted with 0-3 halogens on each carbon.

Oxidation of mixtures of thioureas: Part X - A study of the steric and inductive effects of alkyl groups

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