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Tert-butyl (5-hydroxypentyl)(methyl)carbamate is a chemical compound that features a combination of a tert-butyl group, a carbamate functional group, and a hydroxypentyl group. It is known for its effectiveness as a carbamate insecticide in agricultural applications, characterized by its low toxicity to mammals and enhanced stability and efficacy due to the attached methyl group.

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  • 1373210-02-6 Structure
  • Basic information

    1. Product Name: tert-butyl (5-hydroxypentyl)(methyl)carbamate
    2. Synonyms: tert-butyl (5-hydroxypentyl)(methyl)carbamate;N-Boc 5-(methylamino)pentan-1-ol
    3. CAS NO:1373210-02-6
    4. Molecular Formula:
    5. Molecular Weight: 217.309
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1373210-02-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: tert-butyl (5-hydroxypentyl)(methyl)carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl (5-hydroxypentyl)(methyl)carbamate(1373210-02-6)
    11. EPA Substance Registry System: tert-butyl (5-hydroxypentyl)(methyl)carbamate(1373210-02-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1373210-02-6(Hazardous Substances Data)

1373210-02-6 Usage

Uses

Used in Agricultural Industry:
Tert-butyl (5-hydroxypentyl)(methyl)carbamate is used as a carbamate insecticide for effectively targeting and controlling a variety of pests. Its low toxicity to mammalian species makes it a preferred choice for pest management in agriculture, ensuring both the safety of the environment and the effectiveness of pest control measures. tert-butyl (5-hydroxypentyl)(methyl)carbamate's versatility offers a safe and efficient solution for maintaining crop health and productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1373210-02-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,2,1 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1373210-02:
(9*1)+(8*3)+(7*7)+(6*3)+(5*2)+(4*1)+(3*0)+(2*0)+(1*2)=116
116 % 10 = 6
So 1373210-02-6 is a valid CAS Registry Number.

1373210-02-6Relevant articles and documents

Functionalized Polyhydroquinolines from Amino Acids Using a Key One-Pot Cyclization Cascade and Application to the Synthesis of (±)-Δ7-Mesembrenone

Bélanger, Guillaume,Gallagher-Duval, Shawn,Lapointe, Vincent

supporting information, p. 8606 - 8611 (2021/11/17)

Substituted polyhydroquinolines are ubiquitous skeletal cores found in drugs and bioactive natural products. As a new route to access this motif, we successfully developed a one-pot cyclization cascade with high chemocontrol and diastereoselectivity. The sequence generates two cycles, three carbon-carbon bonds, and an all-carbon quaternary center in a highly convergent process. Functionalized polyhydroquinolines and congeners can be accessed from commercially available amino acids. This versatile and robust strategy was applied to the synthesis of (±)-Δ7-mesembrenone.

HETEROBIFUNCTIONAL MOLECULES AS TEAD INHIBITORS

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Paragraph 0263-0264; 0402-0403, (2021/09/11)

The invention relates to compounds and methods of using said compounds, as well as pharmaceutical compositions containing such compounds, for treating diseases and conditions mediated by TEAD, such as cancer.

DEGRADATION OF BRUTON'S TYROSINE KINASE (BTK) BY CONJUGATION OF BTK INIDBITORS WITH E3 LIGASE LIGAND AND METHODS OF USE

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Paragraph 0280; 0283, (2021/02/05)

Disclosed herein are novel bifunctional compounds formed by conjugating BTK inhibitor moieties with E3 ligase Ligand moieties, which function to recruit targeted proteins to E3 ubiquitin ligase for degradation, and methods of preparation and uses thereof.

CGRP ANTAGONIST COMPOUNDS

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Page/Page column 48, (2020/12/30)

The disclosures herein relate to novel compounds of Formula (1): and salts thereof, wherein A1, A2, Q, X, R1, R2 and R3 are defined herein, and their use in treating, preventing, ameliorating, control

IRAK DEGRADERS AND USES THEREOF

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, (2019/07/10)

The present invention provides compounds, compositions thereof, and methods of using the same.

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