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338990-31-1

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  • N-Methyl-N-(3-[((N-tert-butoxycarbonyl-N-methylamino)acetoxy)methyl]pyridin-2-yl)carbamic acid 1-chloroethyl ester CAS No.:338990-31-1

    Cas No: 338990-31-1

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  • N-Methyl-N-(3-[((N-tert-butoxycarbonyl-N-methylamino)acetoxy)methyl]pyridin-2-yl)carbamic acid 1-chloroethyl ester Cas 338990-31-1

    Cas No: 338990-31-1

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  • N-Methyl-N-{3-{[(N-tert-butoxycarbonyl-N-methylamino)-acetoxy]-methyl}-pyridin-2-yl}-carbamic acid 1-chloroethyl ester

    Cas No: 338990-31-1

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  • N-Methyl-N-(3-[((N-tert-butoxycarbonyl-N-methylamino)acetoxy)methyl]pyridin-2-yl)carbamic acid 1-chloroethyl ester

    Cas No: 338990-31-1

  • USD $ 500.0-500.0 / Gram

  • 1000 Gram

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  • Hebei yanxi chemical co.,LTD.
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338990-31-1 Usage

General Description

The chemical "Glycine, N-[(1,1-diMethylethoxy)carbonyl]-N-Methyl-, [2-[[(1-chloroethoxy)carbonyl]MethylaMino]-3-pyridinyl]Methyl ester" is a complex compound with several functional groups. It contains a glycine moiety, with a protective group of 1,1-diMethylethoxy and N-[(1-chloroethoxy)carbonyl]MethylaMino attached to the N-Methyl group. Additionally, it has an ester group connected to a 3-pyridinylMethyl moiety. This chemical may have applications in pharmaceuticals or organic synthesis due to its unique structure and functional groups, and it would likely require extensive characterization and testing for specific uses.

Check Digit Verification of cas no

The CAS Registry Mumber 338990-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,8,9,9 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 338990-31:
(8*3)+(7*3)+(6*8)+(5*9)+(4*9)+(3*0)+(2*3)+(1*1)=181
181 % 10 = 1
So 338990-31-1 is a valid CAS Registry Number.

338990-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Methyl-N-(3-[((N-tert-butoxycarbonyl-N-methylamino)acetoxy)methyl]pyridin-2-yl)carbamic acid 1-chloroethyl ester

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:338990-31-1 SDS

338990-31-1Relevant articles and documents

Prodrugs of baloxvir and derivatives thereof and preparation method and application of prodrugs

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Paragraph 0047-0050, (2021/05/05)

The present invention provides a compound having a structure represented by formula (I), a stereoisomer thereof, or a pharmaceutically acceptable salt thereof, and a preparation method and use thereof, where X, Y, Z, R1, R2, R3, R4, R5, R6, R7, R8, (R9) m in the formula (I) are defined as in the description and claims of the present invention. The compound is a prodrug of baloxavir and a derivative thereof, and the bioavailability of the compound is greatly improved compared with the bioavailability of the existing baloxavir marboxil. The compound is better than Baloxavir marboxil in the aspects of reducing the dosage, reducing the side effect of the medicine and improving the medicine effect, and can be used as a medicine for treating and/or preventing influenza virus infectious diseases.

INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE AND METHODS OF THEIR USE

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Page/Page column 105; 106; 107, (2019/07/20)

The present invention provides a compound of formula (II): an inhibitor of indoleamine 2,3-dioxygenase (IDO), which may be used as medicaments for the treatment of proliferative disorders, such as cancer, viral infections and/or autoimmune diseases. Its prodrugs are disclosed.

N-substituted carbamoyloxyalkyl-azolium derivatives

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Page/Page column 21-22; 36, (2010/02/09)

N-substituted carbamoyloxyalkyl-azolium derivatives which have antifungal activity and are useful for the treatment of fungal diseases.

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