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5,6-bis(phenylhydrazinylidene)hexane-2,3,4-triol is a complex organic compound with the molecular formula C18H20N4O3. It is characterized by a hexane backbone with two phenylhydrazine groups attached to the 5th and 6th carbon atoms, and three hydroxyl groups at the 2nd, 3rd, and 4th carbon positions. 5,6-bis(phenylhydrazinylidene)hexane-2,3,4-triol is known for its potential applications in various fields, such as pharmaceuticals and chemical research, due to its unique structure and reactivity. It is often synthesized through multi-step processes involving the reaction of appropriate precursors and can be used as a building block for more complex molecules or as a reagent in chemical transformations. The compound's properties, such as solubility and stability, can vary depending on the specific conditions and environment in which it is used.

6035-61-6

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6035-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6035-61-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,3 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6035-61:
(6*6)+(5*0)+(4*3)+(3*5)+(2*6)+(1*1)=76
76 % 10 = 6
So 6035-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H22N4O3/c1-13(23)17(24)18(25)16(22-21-15-10-6-3-7-11-15)12-19-20-14-8-4-2-5-9-14/h2-13,17-18,20-21,23-25H,1H3

6035-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-bis(phenylhydrazinylidene)hexane-2,3,4-triol

1.2 Other means of identification

Product number -
Other names arabino-6-Desoxy-[2]hexosulose-bis-phenylhydrazon

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:6035-61-6 SDS

6035-61-6Relevant academic research and scientific papers

Highly Stereoselective Grignard Reaction of an Aldopyranose: A Simple Synthesis of 6-Deoxy-D-idose from D-Xylose

Tsuda, Yoshisuke,Nunozawa, Tetsuji,Yoshimoto, Kimihiro

, p. 3223 - 3231 (2007/10/02)

Grignard reaction of 2,3,4-tri-O-benzyl-D-xylopyranose yielded a single product with very high stereoselectivity.A threo relationship of the newly created chiral center with respect to C2 was established by converting the product into the δ-lactone of D-ido configuration, then to the unsaturated lactone of threo configuration.The result made possible a stereoselective synthesis of 6-deoxy-D-idose from D-xylose in a small number of steps.Models accounting for the high stereoselectivity in the Grignard reaction of aldoses are discussed.Keywords - Grignard reaction; stereoselectivity; configuration of unsaturated lactones; 2,3,4-tri-O-benzyl-D-xylose; 1-deoxy-D-sorbose; 6-deoxy-D-iono-1,5-lactone; 6-deoxy-D-idose; stereocontrol models

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