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Trans-Tert-Butyl 2-(Hydroxymethyl)-4-Methylpyrrolidine-1-Carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

220047-75-6

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220047-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220047-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,0,4 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 220047-75:
(8*2)+(7*2)+(6*0)+(5*0)+(4*4)+(3*7)+(2*7)+(1*5)=86
86 % 10 = 6
So 220047-75-6 is a valid CAS Registry Number.

220047-75-6SDS

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 (2S,4R)-N-tert-butyloxycarbonyl-2-hydroxymethyl-4-methylpyrrolidine

1.2 Other means of identification

Product number -
Other names N-tert-butyloxycarbonyl-(2S,4R)-2-hydroxymethyl-4-methylpyrrolidine

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:220047-75-6 SDS

220047-75-6Upstream product

220047-75-6Relevant academic research and scientific papers

Reciprocity of steric and stereoelectronic effects in the collagen triple helix

Shoulders, Matthew D.,Hodges, Jonathan A.,Raines, Ronald T.

, p. 8112 - 8113 (2007/10/03)

In previous work, we demonstrated that 4-fluoroproline residues can contribute greatly to the conformational stability of the collagen triple helix, and that this stability arises from stereoelectronic effects that fix the pucker of the pyrrolidine ring and thereby preorganize the backbone properly for triple-helix formation. Here, we take a reciprocal approach, demonstrating that the steric effect of a 4-methyl group confers stability similar to that from a 4-fluoro group in the opposite configuration. Such fundamental interplay between steric and stereoelectronic effects is heretofore unknown in proteinsnatural or syntheticand provides a new means to modulate conformational stability. Copyright

Asymmetric hydrogenations for the synthesis of boc-protected 4-alkylprolinols and prolines

Del Valle, Juan R.,Goodman, Murray

, p. 3923 - 3931 (2007/10/03)

The utility of 4-substituted prolinols and their corresponding prolines in peptides, peptidomimetics, and natural products has motivated researchers to find new and efficient routes for their preparation. Herein, we report a general approach to the synthesis of Boc-protected 4-alkylprolinols and prolines via a divergent asymmetric hydrogenation strategy. Intermediate exocyclic olefins were prepared by Wittig-type reactions with ketone 6 and subjected to hydroxyl and sterically directed reductions. The Crabtree catalyst (Ir[COD] PyPCy3PF6) proved to be highly effective in diastereoselective hydrogenations to give trans- substituted pyrrolidines (9). Good facial selectivities were also observed in heterogeneous hydrogenations with Raney-nickel to obtain cis-substituted pyrrolidines (11). Employing this strategy, we describe the synthesis of novel prolinol and proline-based building blocks for incorporation into biologically relevant peptidomimetics.

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