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GCLE

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Company Name: Hefei Lbao Physical & Chemical Science Co.,Ltd
Tel: +1-5184799099
Email: lbaochemicals@gmail.com
Products Intro: Product Name:GCLE
CAS:104146-10-3
Purity:98% Package:1kg;
Company Name: Capot Chemical Co.,Ltd.
Tel: +86-(0)57185586718; +8613336195806
Email: sales@capot.com
Products Intro: Product Name:GCLE
CAS:104146-10-3
Purity:NLT 98% Package:100G;1KG;100KG
Company Name: Shanghai Daken Advanced Materials Co.,Ltd
Tel: +86-2158073036
Email: info@dakenam.com
Products Intro: Product Name:GCLE
CAS:104146-10-3
Package:1KG,5KG,10KG
Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: +86-0371-55170693 +86-19937530512
Email: info@tianfuchem.com
Products Intro: Product Name:GCLE
CAS:104146-10-3
Purity:99% Package:25KG;5KG;1KG
Company Name: Nanjing ChemLin Chemical Industry Co., Ltd.
Tel: 025-83697070
Email: product@chemlin.com.cn
Products Intro: CAS:104146-10-3
Purity:98% Package:g-Kg Remarks:White or light yellow crystal or crystalline powder

GCLE manufacturers

  • GCLE
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  • 2026-03-14
  • CAS:104146-10-3
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  • Purity: 0.99
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  • GCLE
  • GCLE pictures
  • $0.00 / 1kg
  • 2026-03-14
  • CAS:104146-10-3
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: Customise
GCLE Basic information
Product Name:GCLE
Synonyms:(4-methoxyphenyl)methylester,(6r-trans)-7-((phenylacetyl)amino);2,0)oct-2-ene-2-carboxylicacid,3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo(;7-phenylacetamido-3-chloromethylcephem-4-carbonicacidp-methoxybenzylester;7-PHENYLACETAMINO-3-CHLOROMETHYL-3-CEPHEM4-CARBOXYLIC ACID P-METHOXYBENZYL ESTER;7-PHENYLACETAMIDE-3-CHLOROMETHYL-3-CEPHEM-4-CARBOXYLIC ACID P-METHOXYBENZYL ESTER;7-PHENYLACETAMIDE-3-CHLOROMETHYL-CEPHALOSPORANIC ACID P-METHOXYBENZYL ESTER;7-PHENYLACETAMIDO-3-CHLOROMETHYL-3-CEPHEM-4-CARBOXYLIC ACID 4-METHOXYBENZYL ESTER;GCLE
CAS:104146-10-3
MF:C24H23ClN2O5S
MW:486.97
EINECS:403-040-0
Product Categories:Chiral Reagents;Heterocycles;Intermediates;Intermediates & Fine Chemicals;Pharmaceuticals;1;3
Mol File:104146-10-3.mol
GCLE Structure
GCLE Chemical Properties
Melting point 153-155°C
Boiling point 756.6±60.0 °C(Predicted)
density 1.41±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly, Heated, Sonicated)
form Solid
pka13.61±0.60(Predicted)
color White to Off-White
Optical RotationConsistent with structure
InChIKeyKFCMZNUGNLCSJQ-NFBKMPQASA-N
SMILESN12[C@@]([H])([C@H](NC(CC3=CC=CC=C3)=O)C1=O)SCC(CCl)=C2C(OCC1=CC=C(OC)C=C1)=O
CAS DataBase Reference104146-10-3(CAS DataBase Reference)
Safety Information
RTECS XI0369883
HS Code 2941.90.3000
MSDS Information
GCLE Usage And Synthesis
Chemical PropertiesWhite Solid
Uses4-Methoxybenzyl 3-Chloromethyl-7-(2-phenylacetamido)-3-cephem-4-carboxylate is a key intermediate of cephem compounds.
UsesA key intermediate of cephem compounds.
Synthesis
1-Azetidineacetic acid, α-[1-(chloromethyl)ethenyl]-2-(2,2-dioxido-2-phenyldithio)-4-oxo-3-[(2-phenylacetyl)amino]-, (4-methoxyphenyl)methyl ester, (αR,2R,3R)-

131903-39-4

GCLE

104146-10-3

The general procedure for the synthesis of (6R,7R)-3-(chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thiophene-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid-4-methoxybenzyl ester, using the compound (CAS:131903-39-4) as a starting material, was as follows: in 2000 mL dioxane, 120 g of sodium bicarbonate ( 1.43 mol) and 200 g of azodioxanone sulfinic acid intermediate (0.336 mmol) and stirred at 10 to 15 °C. 30 g of chlorine gas (0.422 mol) was slowly passed for about 3 h. The reaction progress was monitored by HPLC until the peak area of the feedstock dropped below 0.5%. The passage of chlorine gas was stopped, sodium bicarbonate was removed by filtration and dioxane was recovered under vacuum. 2000 mL of methanol was added to dissolve the residue and the reaction temperature was maintained at 0-5 °C. Subsequently, a 900 mL methanol solution of 18 g sodium methanolate (0.34 mol) was added and the reaction was maintained at 0~5 °C for 30 min. The pH of the reaction system was adjusted to 4~6 with 10% hydrochloric acid and stirring was continued at 0~5°C for 1 hour. After completion of the reaction, the product was collected by filtration, washed with water and methanol sequentially, and dried to give 125 g of GCLE in 76.3% yield and ≥94% purity.

References[1] Patent: CN107033162, 2017, A. Location in patent: Paragraph 0024; 0027
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