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906453-98-3

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906453-98-3 Usage

General Description

(R)-3-(benzyloxy)hex-5-enamide is a chemical compound with the formula C16H19NO2. It is a chiral compound, meaning it has a non-superimposable mirror image, and the (R) designation indicates the absolute configuration of the molecule. (R)-3-(BENZYLOXY)HEX-5-ENAMIDE contains a hex-5-enamide group, in which a primary amide is attached to a 5-carbon chain with a double bond, and a benzyloxy group, in which a benzene ring is connected to an oxygen atom that is in turn attached to the 3-carbon of the chain. The compound may have applications in organic synthesis and pharmaceutical research due to its unique structure and potential biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 906453-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,4,5 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 906453-98:
(8*9)+(7*0)+(6*6)+(5*4)+(4*5)+(3*3)+(2*9)+(1*8)=183
183 % 10 = 3
So 906453-98-3 is a valid CAS Registry Number.

906453-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-benzyloxy-hex-5-enoic acid

1.2 Other means of identification

Product number -
Other names 3-benzyloxy-hex-5-enoic acid

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:906453-98-3 SDS

906453-98-3Relevant articles and documents

Eight-step synthesis of routiennocin

Matsumotoa, Kenji,Kozmina, Sergey A.

supporting information; experimental part, p. 557 - 560 (2009/04/11)

Routiennocin is a member of a family of polycyclic pyrrole ether antibiotics that simultaneously uncouple oxidative phosphorylation and inhibit ATPase as a result of selective complexation of divalent metal ions. We describe a concise synthesis of routien

Dramatic enhancement of enantioselectivity of biotransformations of β-hydroxy nitriles using a simple O-benzyl protection/docking group

Ma, Da-You,Zheng, Qi-Yu,Wang, De-Xian,Wang, Mei-Xiang

, p. 3231 - 3234 (2007/10/03)

Catalyzed by the Rhodococcus erythropolis AJ270 whole cell catalyst, the O-benzylated β-hydroxy alkanenitriles underwent remarkably high enantioselective biotransformations, whereas the biotransformations of free β-hydroxy alkanenitriles gave very low ena

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