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2-Decenoic acid, 6-[(1R)-1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]propyl]-2,8-dimethyl-, phenylmethyl ester, (2E,6R,8S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

506449-80-5

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506449-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 506449-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,6,4,4 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 506449-80:
(8*5)+(7*0)+(6*6)+(5*4)+(4*4)+(3*9)+(2*8)+(1*0)=155
155 % 10 = 5
So 506449-80-5 is a valid CAS Registry Number.

506449-80-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-(6R,8S)-6-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-2,8-dimethyl-dec-2-enoic acid benzyl ester

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:506449-80-5 SDS

506449-80-5Relevant academic research and scientific papers

Synthesis of the acyl side chain segment of polyoxypeptins using regioselective ring-opening of chiral 2,3-epoxy alcohol

Makino, Kazuishi,Suzuki, Tatsuya,Awane, Shinobu,Hara, Osamu,Hamada, Yasumasa

, p. 9391 - 9395 (2007/10/03)

The acyl side chain segment 2 contained in polyoxypeptins A (1a) and B (1b), apoptosis-inducing cyclodepsipeptides, was synthesized from chiral 2,3-epoxy alcohol (6), easily prepared by Sharpless asymmetric epoxidation, through a regioselective ring-opening reaction as the key step.

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