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1-(2,3,4,6-tetraacetyl-beta-D-glucopyranosyl)phenobarbital is a chemical compound derived from phenobarbital, a barbiturate medication used as a sedative and for treating seizures and epilepsy. 1-(2,3,4,6-tetraacetyl-beta-D-glucopyranosyl)phenobarbital is modified by attaching a glucose molecule (beta-D-glucopyranosyl) with four acetyl groups to the phenobarbital molecule. This modification is thought to enhance the solubility and bioavailability of the compound, potentially increasing its effectiveness in medical applications. The addition of acetyl groups to the glucose molecule also serves to protect it from enzymatic degradation, allowing for a more sustained release of phenobarbital in the body. This chemical compound may hold promise for the development of new pharmaceutical products for the treatment of neurological disorders and other conditions where phenobarbital is indicated.

72209-11-1

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72209-11-1 Usage

Uses

Used in Pharmaceutical Industry:
1-(2,3,4,6-tetraacetyl-beta-D-glucopyranosyl)phenobarbital is used as a modified barbiturate for the treatment of neurological disorders and conditions where phenobarbital is indicated. 1-(2,3,4,6-tetraacetyl-beta-D-glucopyranosyl)phenobarbital's increased solubility and bioavailability, along with its sustained release properties, make it a potentially more effective option for medical use.
Used in Drug Delivery Systems:
In the field of drug delivery, 1-(2,3,4,6-tetraacetyl-beta-D-glucopyranosyl)phenobarbital can be utilized as a component in the development of novel drug delivery systems. Its enhanced solubility and bioavailability, coupled with the protective acetyl groups on the glucose molecule, may contribute to improved delivery, bioavailability, and therapeutic outcomes for patients requiring treatment with phenobarbital or related compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 72209-11-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,2,0 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72209-11:
(7*7)+(6*2)+(5*2)+(4*0)+(3*9)+(2*1)+(1*1)=101
101 % 10 = 1
So 72209-11-1 is a valid CAS Registry Number.
InChI:InChI=1/C26H30N2O12/c1-6-26(17-10-8-7-9-11-17)23(33)27-25(35)28(24(26)34)22-21(39-16(5)32)20(38-15(4)31)19(37-14(3)30)18(40-22)12-36-13(2)29/h7-11,18-22H,6,12H2,1-5H3,(H,27,33,35)/t18-,19-,20+,21-,22-,26?/m1/s1

72209-11-1SDS

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 [(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(5-ethyl-2,4,6-trioxo-5-phenyl-1,3-diazinan-1-yl)oxan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names TAGPP

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:72209-11-1 SDS

72209-11-1Relevant academic research and scientific papers

Synthesis of N-beta-D-glucopyranosyl derivatives of barbital, phenobarbital, metharbital, and mephobarbital.

Soine,Soine,England,Overton,Merat

, p. 105 - 113 (1989)

The condensation of per(trimethyl)silylbarbital and -phenobarbital with 1,2,3,4,6-penta-O-acetyl-beta-D-glucopyranose in the presence of stannic chloride in dichloroethane gave moderate yields of the beta-coupled barbiturate N-D-glucopyranosyl derivatives. Reaction of metharbital and mephobarbital under the same conditions was unsuccessful. The homologous N-methylglucosides were prepared by reaction of the barbital and phenobarbital N-glucosyl derivatives with diazomethane. The diastereomers of the phenobarbital and mephobarbital derivatives were resolved by use of C-18 reverse-phase h.p.l.c. 1H- and 13C-n.m.r. spectroscopy, and thermospray 1.c.-m.s. proved to be the most useful methods for characterizing the barbiturate glucosides.

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