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1219194-46-3

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1219194-46-3 Usage

Chemical Properties

Colourless Oil

Uses

1,2,3-Tri-O-benzyl-4-[(benzyloxy)methyl]cyclohex-5-ene-1,2,3,4-tetraol (cas# 1219194-46-3) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 1219194-46-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,1,9 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1219194-46:
(9*1)+(8*2)+(7*1)+(6*9)+(5*1)+(4*9)+(3*4)+(2*4)+(1*6)=153
153 % 10 = 3
So 1219194-46-3 is a valid CAS Registry Number.

1219194-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3-Tri-O-benzyl-4-[(benzyloxy)methyl]cyclohex-5-ene-1,2,3,4-tetraol

1.2 Other means of identification

Product number -
Other names 4,5,6-tris(phenylmethoxy)-1-(phenylmethoxymethyl)cyclohex-2-en-1-ol

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:1219194-46-3 SDS

1219194-46-3Relevant articles and documents

Efficient synthesis of (+)-mk7607 and its c-1 epimer via the stereoselective transposition of a tertiary allylic alcohol

Lim, Chaemin,Baek, Dong Jae,Kim, Deukjoon,Youn, So Won,Kim, Sanghee

supporting information; experimental part, p. 2583 - 2586 (2009/10/23)

These studies provide an efficient and stereoselective synthetic route to (+)-MK7607 and its C-1 epimer from a common intermediate in high overall yields. The synthetic methodologies mainly rely on the stereospecific 1,3-allylic transposition of the hinde

β-acarbose. I. The synthesis of 1-epivalienamine

McAuliffe, Joseph C.,Stick, Robert V.

, p. 193 - 196 (2007/10/03)

Improvements and modifications to a literature procedure for the synthesis of multigram amounts of a derivative of 1-epivalienamine are described. As well, various other derivatives of 1-epivalienamine, of potential use in the synthesis of carba sugars, a

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