N-(2-FUROYL)GLYCINE

Product Name: N-(2-FUROYL)GLYCINE
CAS No.: 5657-19-2
Chemical Name: N-(2-FUROYL)GLYCINE
Synonyms: furoylglycine;furoilglicina;2-furoylglycine;furfuroylglycine;Pyromucuric acid;n-2-furoyl-glycin;AKOS BBS-00000709;N-(2-FUROYL)GLYCINE;N-(2-furoyl)glycinate;n-(2-furanylcarbonyl)-glycin
CBNumber: CB4692896
Molecular Formula: C7H7NO4
Formula Weight: 169.13
MOL File: 5657-19-2.mol

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N-(2-FUROYL)GLYCINE Property

Melting point:: 163-165 °C(lit.)
Boiling point:: 466.0±25.0 °C(Predicted)
Density: 1.367±0.06 g/cm3(Predicted)
storage temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility: DMSO (Slightly), Methanol (Slightly)
form: Solid
pka: 3.66±0.10(Predicted)
color: White to Off-White
Water Solubility: >21.55 mg/mL in Water with ultrasonic;
Stability:: Hygroscopic

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Safety

Hazard Codes: Xi
Risk Statements: 36/37/38
Safety Statements: 26-36
WGK Germany: 2
RTECS: MC0555300
HazardClass: IRRITANT

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC

Product number: F865225
Product name: 2-Furoylglycine
Packaging: 50mg
Price: $95
Updated: 2021/12/16

TRC

Product number: F865225
Product name: 2-Furoylglycine
Packaging: 100mg
Price: $155
Updated: 2021/12/16

TRC

Product number: F865225
Product name: 2-Furoylglycine
Packaging: 2.5g
Price: $860
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: CHM0087813
Product name: 2-(2-FUROYLAMINO)ACETIC ACID
Purity: 95.00%
Packaging: 2.5G
Price: $1468.5
Updated: 2021/12/16

Matrix Scientific

Product number: 049111
Product name: 2-(2-Furoylamino)acetic acid
Packaging: 500mg
Price: $237
Updated: 2021/12/16

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N-(2-FUROYL)GLYCINE Chemical Properties,Usage,Production

Uses

2-Furoylglycine is an intermediate used to prepare non-nucleoside inhibitors of HCV NS5b RNA polymerase. It is also used in the synthesis of benzimidazolylazabicyclooctylethylpiperidines as Ccr5 antagonists for the treatment of HIV infection.

Definition

ChEBI: N-(2-furoyl)glycine is a glycine derivative that is the carboxamide obtained by the formal condensation of the amino group of glycine with 2-furoic acid. It has a role as a human metabolite. It is a N-acylglycine and a member of furans. It is functionally related to a 2-furoic acid. It is a conjugate acid of a N-(2-furoyl)glycinate.

N-(2-FUROYL)GLYCINE Preparation Products And Raw materials

Raw materials

Preparation Products

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N-(2-FUROYL)GLYCINE Suppliers

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5657-19-2, N-(2-FUROYL)GLYCINERelated Search:

FURALAXYL N-(2-FUROYL)GLYCINE 2-[(FURAN-2-CARBONYL)-AMINO]-3-METHYL-BUTYRIC ACID 2-[(FURAN-2-CARBONYL)-AMINO]-3-(4-HYDROXY-PHENYL)-PROPIONIC ACID N-(2-FUROYL)ALANINE 1-(2-FURYLCARBONYL)-4-HYDROXY-2-PYRROLIDINECARBOXYLIC ACID N-(2-FUROYL)GLYCINE METHYL ESTER 2-(FURAN-2-CARBONYL)-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID 1-(FURAN-2-CARBONYL)-4-HYDROXY-PYRROLIDINE-2-CARBOXYLIC ACID METHYL ESTER 2-[(FURAN-2-CARBONYL)-AMINO]-3-PHENYL-PROPIONIC ACID 4-carbamoyl-2-(furan-2-ylformamido)butanoic acid 1-[(5-methylfuran-2-yl)carbonyl]pyrrolidine-2-carboxylic acid AKOS BBS-00007559 4-amino-2-(2-furoylamino)-4-oxobutanoic acid AURORA 673 AURORA 2283 2-(2-FUROYLAMINO)-4-(METHYLTHIO)BUTANOIC ACID [(5-BROMO-FURAN-2-CARBONYL)-AMINO]-ACETIC ACID

n-2-furoyl-glycin

2-(2-furylcarbonylamino)acetic acid

Pyromucuric acid

N-(2-furoyl)glycinate

2-(furan-2-carbonylamino)acetic acid

AKOS BBS-00000709

N-(2-FUROYL)GLYCINE

2-furoylglycine

furfuroylglycine

furoilglicina

furoylglycine

n-(2-furanylcarbonyl)-glycin

n-(2-furanylcarbonyl)glycine

Glycine, N-(2-furanylcarbonyl)-

2-(furan-2-carbonylamino)aceticaci

N-(2-FUROYL)GLYCINE USP/EP/BP

5657-19-2

Specialty Synthesis

Unnatural Amino Acid Derivatives

Peptide Synthesis

Glycine Derivatives

Peptide Synthesis

Unnatural Amino Acid Derivatives