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2-T-BUTYL GLYCOLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50595-15-8

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50595-15-8 Usage

Chemical Properties

White to off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 50595-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,9 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50595-15:
(7*5)+(6*0)+(5*5)+(4*9)+(3*5)+(2*1)+(1*5)=118
118 % 10 = 8
So 50595-15-8 is a valid CAS Registry Number.

50595-15-8SDS

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 tert-Butyl 2-hydroxyacetate

1.2 Other means of identification

Product number -
Other names tert-butyl 2-hydroxyacetate

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:50595-15-8 SDS

50595-15-8Relevant articles and documents

Photolithographic Synthesis of Peptoids

Li, Shuwei,Bowerman, Dawn,Marthandan, Nishanth,Klyza, Stanley,Luebke, Kevin J.,Garner, Harold R.,Kodadek, Thomas

, p. 4088 - 4089 (2007/10/03)

We describe a novel photolithographic approach to the synthesis of peptoids (oligo-N-substituted glycines). This strategy enables the construction of a spatially addressable peptoid microarray, thus providing a potentially powerful tool for the discovery

Domino processes as a tool for recovering substandard reactions. Synthesis and use of nitroacetic acid esters and amides

Scardovi, Noemi,Casalini, Andrea,Peri, Francesca,Righi, Paolo

, p. 965 - 968 (2007/10/03)

(equation presented) Elusive nitroacetic acid esters and amides were obtained through a halogen exchange reaction of the corresponding bromoacetic acid derivatives with polymer-supported nitrite anion. The process is flawed by a side product catalyzed deg

Approaches to the Synthesis of Endothiopeptides: Synthesis of a Thioamide-Containing C-Terminal Bombesin Nonapeptide

Jurayj, Jurjus,Cushman, Mark

, p. 8601 - 8614 (2007/10/02)

Several approaches have been investigated for the synthesis of a bombesin C-terminal nonapeptide analogue AsnGlnTrpAlaValGlyHisLeu-ΨCSNHMet-NH2.A new activated dithioester 16 has been synthesized.Thioacylation of methionine methyl ester with 16 was always

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