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16801-19-7

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16801-19-7 Usage

Physical state

Colorless liquid

Odor

Faintly sweet

Common uses

Organic synthesis, monomer in production of polymers and resins (e.g. epoxy resins), preparation of specialty chemicals and pharmaceuticals

Reactivity

Reactive compound

Hazards

Causes irritation to skin, eyes, and respiratory system, potential carcinogen and mutagen

Handling precautions

Handle with care, follow proper chemical handling and safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 16801-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,0 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16801-19:
(7*1)+(6*6)+(5*8)+(4*0)+(3*1)+(2*1)+(1*9)=97
97 % 10 = 7
So 16801-19-7 is a valid CAS Registry Number.

16801-19-7SDS

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 2-(2-ethenoxyethoxymethyl)oxirane

1.2 Other means of identification

Product number -
Other names ((2-(Ethenyloxy)ethoxy)methyl)oxirane

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:16801-19-7 SDS

16801-19-7Relevant articles and documents

Synthetic aptamer-polymer hybrid constructs for programmed drug delivery into specific target cells

Oh, Seung Soo,Lee, Bongjae F.,Leibfarth, Frank A.,Eisenstein, Michael,Robb, Maxwell J.,Lynd, Nathaniel A.,Hawker, Craig J.,Soh, H. Tom

, p. 15010 - 15015 (2014)

Viruses have evolved specialized mechanisms to efficiently transport nucleic acids and other biomolecules into specific host cells. They achieve this by performing a coordinated series of complex functions, resulting in delivery that is far more efficient than existing synthetic delivery mechanisms. Inspired by these natural systems, we describe a process for synthesizing chemically defined molecular constructs that likewise achieve targeted delivery through a series of coordinated functions. We employ an efficient "click chemistry" technique to synthesize aptamer-polymer hybrids (APHs), coupling cell-targeting aptamers to block copolymers that secure a therapeutic payload in an inactive state. Upon recognizing the targeted cell-surface marker, the APH enters the host cell via endocytosis, at which point the payload is triggered to be released into the cytoplasm. After visualizing this process with coumarin dye, we demonstrate targeted killing of tumor cells with doxorubicin. Importantly, this process can be generalized to yield APHs that specifically target different surface markers.

DETERMINATION OF OPTIMUM CONDITIONS FOR SYNTHESIS OF GLYCIDYL VINYLOXYETHYL ETHER BY MATHEMATICAL EXPERIMENTAL DESIGN

Belozerov, L. E.,Stankevich, V. K.,Ezhova, L. N.,Balakhchi, G. K.,Trofimov, B. A.

, p. 1231 - 1232 (2007/10/02)

Synthesis of glycidyl vinyloxyethyl ether by reaction of ethylene glycol monovinyl ether with epichlorohydrin in the presence of sodium hydroxide has been investigated by mathematical experimental design.

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