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93967-75-0

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93967-75-0 Usage

Description

N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE is a white solid chemical compound that is a derivative of pyrrolidinecarboxylic acid. It belongs to the class of pyrrolidinecarboxylic acid derivatives and is characterized by the presence of a phenoxy group and a BOC (tert-butoxycarbonyl) protecting group attached to the nitrogen atom. This versatile chemical intermediate is used in the synthesis of various pharmaceutical and agrochemical products, making it a valuable component in the development of new drugs and chemical compounds.

Uses

Used in Pharmaceutical Industry:
N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE is used as a chemical intermediate for the synthesis of various pharmaceutical products. Its unique structure, including the phenoxy group and the BOC protecting group, allows for the development of new drugs targeting specific biological pathways. N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE plays a crucial role in the creation of innovative medications with potential therapeutic benefits.
Used in Agrochemical Industry:
N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE is also used as a chemical intermediate in the synthesis of agrochemical products. Its versatile nature enables the development of new agrochemicals with improved properties, such as enhanced effectiveness, reduced environmental impact, and targeted pest control. N-BOC-METHYL(2S,4S)-4-PHENOXY-2-PYRROLIDINECARBOXYLATE contributes to the advancement of sustainable agricultural practices by providing a foundation for the creation of innovative agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 93967-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,6 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93967-75:
(7*9)+(6*3)+(5*9)+(4*6)+(3*7)+(2*7)+(1*5)=190
190 % 10 = 0
So 93967-75-0 is a valid CAS Registry Number.

93967-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,4S)-2-methyl-1-[(2-methylpropan-2-yl)oxycarbonyl]-4-phenoxypyrrolidine-2-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:93967-75-0 SDS

93967-75-0Relevant articles and documents

SMAC MIMETICS USED AS IAP INHIBITORS AND USE THEREOF

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Paragraph 0182; 0184, (2020/12/10)

Disclosed are a class of SMAC mimetics used as IAP inhibitors, and in particular disclosed are compounds as shown in formula (I), isomers thereof, and pharmaceutically acceptable salts thereof. The IAP inhibitors are drugs for treating cancers, in particu

VLA-4 INHIBITORS

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, (2008/06/13)

The present invention relates to a compound represented by the following formula (I): (wherein, W represents WA-A1 -WB - (in which, WA is substituted or unsubstituted aryl, etc., A1 is -NR1-, single bond, -C(O)-, etc., and WB is substituted or unsubstituted arylene, etc.), R is single bond, -NH-, -OCH2-, alkenylene, etc., X is -C(O) -CH2-, etc., and M is, for example, the following formula: (in which, R11, R12 and R13 each independently represents hydrogen, hydroxyl, amino, halogen, etc., R14 is hydrogen or lower alkyl, Y represents -CH2-O-, etc., Z is substituted or unsubstituted arylene, etc., A2 is single bond, etc, and R10 is hydroxyl or lower alkoxy)), or salt thereof; and a medicament containing the same. This compound or salt thereof selectively inhibits binding of cell adhesion molecules to VAL-4 and exhibits high bioavailability so that it is useful as a preventive and/or remedy for inflammatory diseases, autoimmune diseases, metastasis, bronchial asthma, rhinostenosis, diabetes, and the like.

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