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2-HydroxyMethyl-pyrrolidine-1-carboxylic acid benzyl ester is a versatile chemical compound that serves as a benzyl ester derivative of 2-hydroxymethyl pyrrolidine-1-carboxylic acid, an important building block in the synthesis of various drugs and bioactive compounds. 2-HydroxyMethyl-pyrrolidine-1-carboxylic acid benzyl ester exhibits potential medicinal properties and is valuable in organic synthesis and pharmaceutical research.
Used in Pharmaceutical Research:
2-HydroxyMethyl-pyrrolidine-1-carboxylic acid benzyl ester is used as a key intermediate for the synthesis of various drugs and bioactive compounds, contributing to the development of novel therapeutic agents.
Used in Organic Synthesis:
2-HydroxyMethyl-pyrrolidine-1-carboxylic acid benzyl ester is used as a valuable intermediate in the synthesis of other organic compounds, facilitating the creation of a wide range of chemical products.

86954-05-4

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86954-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86954-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,5 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86954-05:
(7*8)+(6*6)+(5*9)+(4*5)+(3*4)+(2*0)+(1*5)=174
174 % 10 = 4
So 86954-05-4 is a valid CAS Registry Number.

86954-05-4SDS

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 benzyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names N-<(Benzyloxy)carbonyl>-2-(hydroxymethyl)pyrrolidine

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:86954-05-4 SDS

86954-05-4Relevant academic research and scientific papers

First synthesis process of octahydro-5H-pyrrolo[1,2-A][1,4]diazepin-5-one

-

, (2019/01/05)

The invention relates to a first synthesis process of octahydro-5H-pyrrolo[1,2-A][1,4]diazepin-5-one. The process comprises the steps of subjecting DL-proline, which serves as a starting material, tocarboxyl reduction so as to obtain pyrrolidin-2-methanol

A library of conformationally restricted saturated heterocyclic sulfonyl chlorides

Zhersh, Sergey,Buryanov, Volodymyr V.,Karpenko, Oleksandr V.,Grygorenko, Oleksandr O.,Tolmachev, Andrey A.

scheme or table, p. 3669 - 3674 (2011/12/16)

An approach to the synthesis of conformationally restricted saturated heterocyclic sulfonyl chlorides is described. Being guided by the principle of diversity-oriented conformational restriction, a mini-library of saturated heterocyclic sulfonyl chlorides

Synthesis of alkaloid analogues from β-amino alcohols by β-fragmentation of primary alkoxyl radicals

Boto, Alicia,Hernandez, Dacil,Hernandez, Rosendo,Montoya, Adriana,Suarez, Ernesto

, p. 325 - 334 (2007/10/03)

The fragmentation of primary alkoxyl radicals is usually a minor process with respect to hydrogen abstraction and other competing reactions. However, when β-amino alcohols were used as substrates, the scission proceeded in good to excellent yields and no side reactions were observed. The fragmentation can be coupled with an allylation or alkylation reaction, to give alkaloid analogues and functionalized nitrogen heterocycles. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

Src kinase inhibitor compounds

-

, (2008/06/13)

Pyrimidine compounds (Formula I), or their pharmaceutically acceptable salts, hydrates, solvates, crystal forms and individual diastereomers, and pharmaceutical compositions including the same, which are inhibitors of tyrosine kinase enzymes, and as such are useful in the prophylaxis and treatment of protein tyrosine kinase-associated disorders, such as immune diseases, hyperproliferative disorders and other diseases in which inappropriate protein kinase action is believed to play a role, such as cancer, angiogensis, atheroscelerosis, graft rejection, rheumatoid arthritis and psoriasis.

Efficient and chemoselective cleavage of TBS ethers by a sub-stoichiometric amount of decaborane

Jeong, Yeon Joo,Lee, Ji Hee,Park, Eun Soo,Yoon, Cheol Min

, p. 1223 - 1225 (2007/10/03)

TBS ethers od aliphatic alcohols in THF-MeOH (or methanol) were deprotected chemoselectively to the corresponding alcohols using a sub-stoichiometric amount of decaborane at rt under nitrogen in high yields.

Angiotensin II antagonists

-

, (2008/06/13)

This invention provides novel heterocyclic derivatives, their pharmaceutical formulations, and their use for antagonizing angiotensin II receptors in mammals.

Angiotensin II antagonist intermediates

-

, (2008/06/13)

This invention provides novel heterocyclic derivatives, their pharmaceutical formulations, and their use for antagonizing angiotensin II receptors in mammals.

Benzazepine and benzothiazepine derivatives

-

, (2008/06/13)

Vasodilating activity is exhibited by compounds having the formula STR1 wherein X can be --S--or --CH2 --; and R2 is STR2 depending upon the definition of X.

A Synthesis of a New Type of Alkoxycarbonylating Reagents from 1,1-Bis Carbonate (BTBC) and Their Reactions

Takeda, Kazuyoshi,Tsuboyama, Kanoko,Hoshino, Mitsuho,Kishino, Miyuki,Ogura, Haruo

, p. 557 - 560 (2007/10/02)

1,1'-Bis carbonate (BTBC) was prepared from 1-hydroxy-6-trifluoromethylbenzotriazole and trichloromethyl chloroformate (trichloromethyl carbonochloridate).The reaction of BTBC and alcohols afforded the corresponding acti

p-ANISYL GROUP: A VERSATILE PROTECTING GROUP FOR PRIMARY ALCOHOLS

Fukuyama, Tohru,Laird, Alison A.,Hotchkiss, Lia M.

, p. 6291 - 6292 (2007/10/02)

A primary alcohol can be protected as a highly stable p-anisyl ether, which undergoes mild oxidative deprotection by ceric ammonium nitrate.

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