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Propanoic acid, 2-hydroxy-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59854-10-3

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59854-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59854-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,5 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59854-10:
(7*5)+(6*9)+(5*8)+(4*5)+(3*4)+(2*1)+(1*0)=163
163 % 10 = 3
So 59854-10-3 is a valid CAS Registry Number.

59854-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 2-hydroxypropanoate

1.2 Other means of identification

Product number -
Other names tert-butyl D-(-)-lactate

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:59854-10-3 SDS

59854-10-3Downstream Products

59854-10-3Relevant academic research and scientific papers

Ni-Catalyzed C(sp3)–O Arylation of α-Hydroxy Esters

Monteith, John J.,Rousseaux, Sophie A. L.

supporting information, p. 9485 - 9489 (2021/12/09)

A Negishi cross-coupling of α-hydroxy ester derivatives and arylzinc reagents has been developed. This reaction tolerates both primary and secondary C(sp3)–O alcohol precursors and achieves efficient cross-coupling under Ni catalysis without the need for added external metal reductant, photocatalyst, or additives. The arylation of readily accessible C(sp3)–O electrophiles in this operationally simple, rapid, and mild reaction provides a complementary way of accessing desirable α-aryl ester products.

Dearomative [2,3] sigmatropic rearrangement of ammonium ylides followed by 1,4-elimination to form α-(ortho-vinylphenyl)amino acid esters

Tayama, Eiji,Sotome, Sho

supporting information, p. 4833 - 4839 (2018/07/15)

A base-induced dearomative [2,3] sigmatropic rearrangement of amino acid ester-derived ammonium salts followed by 1,4-elimination produced α-(ortho-vinylphenyl)amino acid esters. The reaction of azetidine-2-carboxylic acid-derived ammonium salt, (1S,2S,1′R)-3b, proceeded with a perfect N-to-C chirality transfer to afford α-(ortho-vinylphenyl)azetidine-2-carboxylic acid ester, (R)-5 (99% ee). On the other hand, the reaction of glycine-derived ammonium salt (R)-6a, which involves an efficient chirality transfer from a chiral benzylic carbon to an α-carbon of an ester carbonyl giving the optically active α-(ortho-vinylphenyl)glycine ester, (R)-8a (85% ee), was demonstrated. Although this dearomative [2,3] rearrangement followed by 1,4-elimination has limitations with regard to the structures of the substrates, our method provides unique access to substituted α-arylamino acid derivatives.

A mild, efficient, and inexpensive protocol for the selective deprotection of TBDMS ethers using KHSO4

Arumugam, Pandurangan,Karthikeyan, Ganesan,Perumal, Paramasivan T.

, p. 1146 - 1147 (2007/10/03)

Potassium hydrogensulfate in 30% aq. methanol deprotects a variety of tert-butyldimethylsilyl ethers at room temperature in excellent yields.

Antiglaucoma compositions and methods

-

, (2008/06/13)

The present invention relates to ophthalmological pharmaceutical compositions comprising (benzothiadiazine, benzamide and benzenesulfonyl)phenyl-substituted carboxyalkyl dipeptide compounds and to methods for using said composition in reducing intraocular

Antihypertensive agents

-

, (2008/06/13)

(Benzothiadiazine, benzamido and benzenesulfonyl)phenyl-substituted carboxyalkyl dipeptide compounds are disclosed. Compounds of this invention are useful as antihypertensive agents.

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