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RARECHEM AL CC 1140, with the molecular formula C20H35NO2, is a clear, colorless liquid characterized by a faint odor and a molecular weight of 325.5 g/mol. It is a chemical compound renowned for its high purity and quality, making it a preferred choice in various scientific and industrial applications.
Usage:
Used in Chemical Synthesis:
RARECHEM AL CC 1140 is used as a reagent in chemical synthesis for its ability to facilitate the creation of new compounds and contribute to the advancement of chemical processes.
Used in Pharmaceutical Production:
In the pharmaceutical industry, RARECHEM AL CC 1140 is utilized as a key component in the manufacturing of various drugs, leveraging its chemical properties to enhance the efficacy and quality of medicinal products.
Used in Agrochemical Production:
RARECHEM AL CC 1140 also finds application in the agrochemical sector, where it is employed in the production of agricultural chemicals, contributing to the development of more effective and safer products for crop protection and enhancement.
Used in Other Industrial Products:
Beyond the aforementioned industries, RARECHEM AL CC 1140 is incorporated into the manufacturing processes of a range of other industrial products, capitalizing on its versatile properties to improve product performance and quality.

4702-12-9

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4702-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4702-12-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4702-12:
(6*4)+(5*7)+(4*0)+(3*2)+(2*1)+(1*2)=69
69 % 10 = 9
So 4702-12-9 is a valid CAS Registry Number.

4702-12-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)hexanoic acid

1.2 Other means of identification

Product number -
Other names phthalimidohexanoic acid

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:4702-12-9 SDS

4702-12-9Relevant academic research and scientific papers

A Novel Class of 7-Membered Heterocyclic Compounds

Bauer, Adriano,Borsos, Eszter,Maulide, Nuno

supporting information, p. 3971 - 3974 (2020/05/25)

The work presented herein describes the synthesis of a formerly inaccessible class of heterocyclic compounds. The reaction relies on α-phthalimido-amides, which are readily prepared from amino acids in 2 simple reactions steps. Under amide activation conditions in which classical keteniminium ions are not formed, the nitrile solvent is incorporated into the new fused 7-membered ring system. Due to the absence of a keteniminium intermediate, the stereogenic information in the α-position is fully retained.

Synthesis of Quaternary α-Fluorinated α-Amino Acid Derivatives via Coordinating Cu(II) Catalytic α-C(sp3)-H Direct Fluorination

Wei, Qiang,Ma, Yao,Li, Li,Liu, Qingfei,Liu, Zijie,Liu, Gang

supporting information, p. 7100 - 7103 (2018/11/24)

A coordinating, copper-catalyzed direct α-C(sp3)-H fluorination method has been developed to prepare vital quaternary α-fluorinated α-amino acid derivatives. A Cu(II) catalytic SET oxidative addition mechanism is proposed, involving a key fluoride-coupled Cu(II) charge transfer complex. The protocol can tolerate a rich variety of α-amino acids, for which the auxiliary group is removed in high yield and substituted for the direct preparation of dipeptide derivatives with detachable, single absolute configurations of the target compounds.

Site-Selective Aliphatic C-H Chlorination Using N-Chloroamides Enables a Synthesis of Chlorolissoclimide

Quinn, Ryan K.,K?nst, Zef A.,Michalak, Sharon E.,Schmidt, Yvonne,Szklarski, Anne R.,Flores, Alex R.,Nam, Sangkil,Horne, David A.,Vanderwal, Christopher D.,Alexanian, Erik J.

supporting information, p. 696 - 702 (2016/02/03)

Methods for the practical, intermolecular functionalization of aliphatic C-H bonds remain a paramount goal of organic synthesis. Free radical alkane chlorination is an important industrial process for the production of small molecule chloroalkanes from simple hydrocarbons, yet applications to fine chemical synthesis are rare. Herein, we report a site-selective chlorination of aliphatic C-H bonds using readily available N-chloroamides and apply this transformation to a synthesis of chlorolissoclimide, a potently cytotoxic labdane diterpenoid. These reactions deliver alkyl chlorides in useful chemical yields with substrate as the limiting reagent. Notably, this approach tolerates substrate unsaturation that normally poses major challenges in chemoselective, aliphatic C-H functionalization. The sterically and electronically dictated site selectivities of the C-H chlorination are among the most selective alkane functionalizations known, providing a unique tool for chemical synthesis. The short synthesis of chlorolissoclimide features a high yielding, gram-scale radical C-H chlorination of sclareolide and a three-step/two-pot process for the introduction of the β-hydroxysuccinimide that is salient to all the lissoclimides and haterumaimides. Preliminary assays indicate that chlorolissoclimide and analogues are moderately active against aggressive melanoma and prostate cancer cell lines.

Substituent effects on regioselective intramolecular oxidation of unactivated C-H bonds: Stereoselective synthesis of substituted tetrahydropyrans

Wong, Man-Kin,Chung, Nga-Wai,He, Lan,Yang, Dan

, p. 158 - 162 (2007/10/03)

Our previously reported intramolecular δ-selective C-H bond oxidation by dioxiranes, generated in situ from activated ketones, offers a novel approach to the synthesis of tetrahydropyrans. To synthesize substituted tetrahydropyrans in a stereoselective manner, we examined the effects of alkyl, nitrogen, and oxygen substituents at the α-,β-, and γ-sites of ketones on the stereoselectivities of intramolecular C-H bond oxidation reactions. Ketones 1-4 with a methyl group at the α-, β-, or γ-site showed the diastereo-selectivities that agreed with the trans/cis ratio predicted by considering steric interactions in the transition states. Furthermore, ketones 5 and 6 carrying a bulky phthalimido group at the α- and the β-sites, respectively, exhibited excellent stereoselectivity, each affording only one diastereomer. However, ketones 9 and 10 bearing β-oxygen substituents gave reversed stereoselectivity as compared to those with β-alkyl or nitrogen substituents, possibly because of the hydrogen bonding interaction in the transition state. For ketones 12 and 13, both bearing methyl and silyloxy groups, the hydrogen bonding interaction was probably more important than the steric effect on the diastereoselectivity of intramolecular oxidation of C-H bonds.

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