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CAS

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1787261-03-3

Tert-butyl (4-(2-hydroxypropan-2-yl)phenyl)carbamate is a chemical compound with the molecular formula C14H23NO3. It is a carbamate ester characterized by its tert-butyl and phenyl groups, as well as a hydroxypropan-2-yl moiety. tert-butyl (4-(2-hydroxypropan-2-yl)phenyl)carbamate is known for its ability to protect the skin from the harmful effects of ultraviolet radiation, making it a valuable ingredient in sunscreen and cosmetic products.

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  • 1787261-03-3 Structure

  • Basic information

    1. Product Name: tert-butyl (4-(2-hydroxypropan-2-yl)phenyl)carbamate
    2. Synonyms:
    3. CAS NO:1787261-03-3
    4. Molecular Formula:
    5. Molecular Weight: 251.326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1787261-03-3.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 (4-(2-hydroxypropan-2-yl)phenyl)carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl (4-(2-hydroxypropan-2-yl)phenyl)carbamate(1787261-03-3)
    11. EPA Substance Registry System: tert-butyl (4-(2-hydroxypropan-2-yl)phenyl)carbamate(1787261-03-3)

  • 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: 1787261-03-3(Hazardous Substances Data)

1787261-03-3 Usage

Uses

Used in Sunscreen and Cosmetic Products:
Tert-butyl (4-(2-hydroxypropan-2-yl)phenyl)carbamate is used as a UV absorber for its ability to protect the skin from the harmful effects of ultraviolet radiation. This helps in preventing skin damage and reduces the risk of skin cancer.
Used in Photostabilization:
Tert-butyl (4-(2-hydroxypropan-2-yl)phenyl)carbamate is used as a photostabilizer in various products. It prevents the degradation of other chemicals in the presence of sunlight, thus prolonging the shelf life and efficacy of the products it is included in. This is particularly important in industries where product stability and longevity are crucial.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, tert-butyl (4-(2-hydroxypropan-2-yl)phenyl)carbamate may also have potential applications in the pharmaceutical industry. Given its chemical structure and properties, it could be used as an intermediate in the synthesis of other pharmaceutical compounds or as a component in drug delivery systems, depending on further research and development in this area.

Check Digit Verification of cas no

The CAS Registry Mumber 1787261-03-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,8,7,2,6 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1787261-03:
(9*1)+(8*7)+(7*8)+(6*7)+(5*2)+(4*6)+(3*1)+(2*0)+(1*3)=203
203 % 10 = 3
So 1787261-03-3 is a valid CAS Registry Number.

1787261-03-3Downstream Products

1787261-03-3Relevant articles and documents

ROR GAMMA (RORY) MODULATORS

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Page/Page column 42, (2015/06/18)

The present invention relates to compounds according to Formula I: Wherein: A11 - A14 are N or CR11, CR12, CR13, CR14, respectively, with the proviso that no more than two of the four positions A can be simultaneously N; R1 is C(1-6)alkyl, C(3-6)cycloalkyl, C(3-6)cycloalkylC(1 -3)alkyl, (di)C(1-6)alkylamino, (di)C(3-6)cycloalkylamino or (di)(C(3-6)cycloalkylC(1 -3)alkyl)amino, with all carbon atoms of alkyl groups optionally substituted with one or more F and all carbon atoms of cycloalkyl groups optionally substituted with one or more F or methyl; R2 and R3 are independently H, F, methyl, ethyl, hydroxy, methoxy or R2 and R3 together is carbonyl, all alkyl groups, if present, optionally being substituted with one or more F; R4 is H or C(1-6)alkyl; R5 is H, hydroxyethyl, methoxyethyl, C(1-6)alkyl, C(6-10)aryl, C(6-10)arylC(1-3)alkyl, C(1 -9)heteroaryl, C(1-9)heteroarylC(1-3)alkyl, C(3-6)cycloalkyl, C(3-6)cycloalkylC(1 -3)alkyl, C(2-5)heterocycloalkyl or C(2-5)heterocycloalkylC(1-3)alkyl, all groups optionally substituted with one or more F, CI, C(1-2)alkyl, C(1-2)alkoxy or cyano; the sulfonyl group with R1 is represented by one of R7, R8 or R9; the remaining R6-RH are independently H, halogen, C(1-3)alkoxy, (di)C(1-3)alkylamino or C(1-6)alkyl, all of the alkyl groups optionally being substituted with one or more F; and Ri5 and Ri6 are independently H, C(1-6)alkyl, C(3-6)cycloalkyl, C(3-6)cycloalkylC(1-3)alkyl, C(6-10)aryl, C(6-10)arylC(1-3)alkyl, C(1-9)heteroaryl, C(1-9)heteroarylC(1-3)alkyl, C(2-5)heterocycloalkyl or C(2-5)heterocycloalkylC(1-3)alkyl, all groups optionally substituted with one or more F, CI, C(1-2)alkyl, C(1-2)alkoxy or cyano. The compounds can be used as inhibitors of RORy and are useful for the treatment of RORy mediated diseases.

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