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917022-13-0

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  • N-[[TRANS-4-[[(4-AMINO-6-CHLORO-2-PYRIMIDINYL)AMINO]METHYL]CYCLOHEXYL]METHYL]-N-[3-[CYCLOHEXYL[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]PROPYL]CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER

    Cas No: 917022-13-0

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  • 917022-13-0 Carbamic acid, N-[[trans-4-[[(4-amino-6-chloro-2-pyrimidinyl)amino]methyl]cyclohexyl]methyl]-N-[3-[cyclohexyl[(1,1-dimethylethoxy)carbonyl]amino]propyl]-, 1,1-dimethylethyl ester

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  • Carbamic acid, N-[[trans-4-[[(4-amino-6-chloro-2-pyrimidinyl)amino]methyl]cyclohexyl]methyl]-N-[3-[cyclohexyl[(1,1-dimethylethoxy)carbonyl]amino]propyl]-, 1,1-dimethylethyl ester

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  • N-[[TRANS-4-[[(4-AMINO-6-CHLORO-2-PYRIMIDINYL)AMINO]METHYL]CYCLOHEXYL]METHYL]-N-[3-[CYCLOHEXYL[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]PROPYL]CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER

    Cas No: 917022-13-0

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  • N-[[trans-4-[[(4-Amino-6-chloro-2-pyrimidinyl)amino]methyl]cyclohexyl]methyl]-N-[3-[cyclohexyl[(1,1-dimethylethoxy)carbonyl]amino]propyl]carbamic acid 1,1-dimethylethyl ester

    Cas No: 917022-13-0

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  • tert-butyl N-[[4-[[(4-amino-6-chloropyrimidin-2-yl)amino]methyl]cyclohexyl]methyl]-N-[3-[cyclohexyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propyl]carbamate

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  • N-[[trans-4-[[(4-Amino-6-chloro-2-pyrimidinyl)amino]methyl]cyclohexyl]methyl]-N-[3-[cyclohexyl[(1,1-dimethylethoxy)carbonyl]amino]propyl]carbamic acid 1,1-dimethylethyl ester

    Cas No: 917022-13-0

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  • Carbamic acid,N-[[trans-4-[[(4-Amino-6-chloro-2-pyrimidinyl)ao]methyl]cyclohexyl]methyl]-N-[3-[cyclohexyl[(1,1-dimethylethoxy)carbonyl]ao]propyl]-,1,1-dimethylethyl ester

    Cas No: 917022-13-0

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917022-13-0 Usage

General Description

This chemical, more commonly known as Peginterferon beta-1a, is a long-acting form of interferon used for the treatment of multiple sclerosis (MS). It is made from combining carbamic acid with several other compounds. Its complex structure includes an amino-6-chloro-2-pyrimidinyl group and a cyclohexyl group with an attached carbonyl group. It's known for its ability to hamper virus activity and help the immune system reduce inflammation, thereby slowing down the progression and reducing the frequency of relapse in patients with MS. However, like any other drugs, it may also elicit side effects like flu-like symptoms, depression, and increases in certain liver enzymes.

Check Digit Verification of cas no

The CAS Registry Mumber 917022-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,0,2 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 917022-13:
(8*9)+(7*1)+(6*7)+(5*0)+(4*2)+(3*2)+(2*1)+(1*3)=140
140 % 10 = 0
So 917022-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C31H53ClN6O4/c1-30(2,3)41-28(39)37(17-10-18-38(24-11-8-7-9-12-24)29(40)42-31(4,5)6)21-23-15-13-22(14-16-23)20-34-27-35-25(32)19-26(33)36-27/h19,22-24H,7-18,20-21H2,1-6H3,(H3,33,34,35,36)/t22-,23-

917022-13-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[[4-[[(4-amino-6-chloropyrimidin-2-yl)amino]methyl]cyclohexyl]methyl]-N-[3-[cyclohexyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propyl]carbamate

1.2 Other means of identification

Product number -
Other names N-[[TRANS-4-[[(4-AMINO-6-CHLORO-2-PYRIMIDINYL)AMINO]METHYL]CYCLOHEXYL]METHYL]-N-[3-[CYCLOHEXYL[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]PROPYL]CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER

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

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More Details:917022-13-0 SDS

917022-13-0Downstream Products

917022-13-0Relevant articles and documents

MOBILIZING CELLS EXPRESSING A TYPE 4 CXC CHEMOKINE RECEPTOR WITH 4-AMINO PYRIMIDINE COMPOUNDS

-

, (2016/04/26)

A method of mobilizing cells expressing the type 4 CXC chemokine receptor into the peripheral circulation by contacting them with an effective amount of a compound of formula (I) shown below (each variable in the formula being defined in the Specification

Pyrimidine compounds

-

Page/Page column 114-115, (2008/06/13)

This invention relates to a method for treating inflammatory diseases or immune diseases, developmental or degenerative diseases, or tissue injuries. The method includes administering to a subject in need thereof an effective amount of one or more compounds of formula (I). Each variable in this formula is defined in the specification.

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