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Methyl 2,3,4-tri-O-acetyl-6-chloro-6-deoxyhexopyranoside is a complex organic chemical compound with the molecular formula C11H15ClO7. It is a derivative of a hexopyranoside, which is a type of sugar molecule, with three acetyl groups (-COCH3) attached to the 2nd, 3rd, and 4th carbon atoms, and a chlorine atom replacing the hydroxyl group (-OH) at the 6th carbon position. methyl 2,3,4-tri-O-acetyl-6-chloro-6-deoxyhexopyranoside is a key intermediate in the synthesis of various pharmaceuticals and biologically active molecules, as it can be further modified to introduce different functional groups or used as a building block in the construction of more complex structures. Its unique structure and reactivity make it a valuable tool in organic synthesis and medicinal chemistry.

6087-46-3

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6087-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6087-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6087-46:
(6*6)+(5*0)+(4*8)+(3*7)+(2*4)+(1*6)=103
103 % 10 = 3
So 6087-46-3 is a valid CAS Registry Number.

6087-46-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [4,5-diacetyloxy-2-(chloromethyl)-6-methoxyoxan-3-yl] acetate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6087-46-3 SDS

6087-46-3Relevant academic research and scientific papers

Active-site engineering of nucleotidylyltransferases and general enzymatic methods for the synthesis of natural and "unnatural" UDP- and TDP-nucleotide sugars

-

, (2008/06/13)

The present invention provides mutant nucleotidylyl-transferases, such as Ep, having altered substrate specificity; methods for their production; and methods of producing nucleotide sugars, which utilize these nucleotidylyl-transferases. The present invention also provides methods of synthesizing desired nucleotide sugars using natural and/or modified Ep or other nucleotidyltransferases; and nucleotide sugars sythesized by the present methods. The present invention further provides new glycosyl phosphates, and methods for making them.

DESIGN AND REACTIVITY OF ORGANIC FUNCTIONAL GROUPS - 2-PYRIDYLSULFONATES AS NUCLEOFUGAL ESTERS: REMARKABLY MILD TRANSFORMATIONS INTO HALIDES AND OLEFINS

Hanessian, Stephen,Kagotani, Masahiro,Komaglou, Kossi

, p. 1115 - 1120 (2007/10/02)

The novel 2-pyridylsulfonate esters are excellent leaving groups for the preparation of bromides and olefins under very mild reaction conditions.Displacements occur with inversion of configuration.

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