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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

a-D-Glucopyranuronic acid, methyl ester, 2,3,4-tris(2-methylpropanoate)1-(2,2,2-trichloroethanimidate)

COC(=O)C1O[C@H](OC(=N)C(Cl)(Cl)Cl)[C@H]([C@H]([C@@H]1OC(=O)C(C)C)OC(=O)C(C)C)OC(=O)C(C)C Request for Quotation
Chemical Name: a-D-Glucopyranuronic acid, methyl ester, 2,3,4-tris(2-methylpropanoate)1-(2,2,2-trichloroethanimidate)
CAS Number: 150607-96-8
Product Number: AG001MRK(AGN-PC-0Q4YCH)
Synonyms:
MDL No:
Molecular Formula: C21H30Cl3NO10
Molecular Weight: 562.8226

Identification/Properties

Properties
MP:
74-75˚C
Storage:
-10 ℃;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
562.818g/mol
XLogP3:
4.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
11
Rotatable Bond Count:
13
Exact Mass:
561.094g/mol
Monoisotopic Mass:
561.094g/mol
Topological Polar Surface Area:
148A^2
Heavy Atom Count:
35
Formal Charge:
0
Complexity:
812
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3,4-Tri-O-isobutyryl-1-O-trichloroacetimidoyl-alpha-D-glucopyranuronic acid methyl ester, also known by its chemical formula [insert formula here], is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in various reactions and processes in the field of chemistry. Due to its unique chemical properties, it is commonly employed as a protective agent in the synthesis of complex organic molecules.This compound is particularly valuable in the protection of hydroxyl groups in carbohydrate chemistry. By selectively masking specific hydroxyl groups with the isobutyryl and trichloroacetimidoyl groups, 2,3,4-Tri-O-isobutyryl-1-O-trichloroacetimidoyl-alpha-D-glucopyranuronic acid methyl ester can facilitate the controlled manipulation of molecular structures. This protective strategy allows chemists to carry out selective transformations on target molecules without unwanted side reactions or cross-reactivity.Furthermore, this compound can be utilized in the preparation of glycosidic linkages and other carbohydrate derivatives. Its strategic incorporation into synthetic pathways enables the efficient construction of complex sugar molecules with high selectivity and yield. By leveraging the unique reactivity of each functional group, chemists can orchestrate intricate chemical transformations to achieve the desired final product.Overall, the application of 2,3,4-Tri-O-isobutyryl-1-O-trichloroacetimidoyl-alpha-D-glucopyranuronic acid methyl ester in chemical synthesis underscores its significance as a valuable tool for organic chemists striving to access new compounds and advance the frontiers of synthetic chemistry.