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2-amino-3'-(2-tert-butoxycarbonylaminoethyl)-5-chloro-benzophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 214977-59-0 Structure
  • Basic information

    1. Product Name: 2-amino-3'-(2-tert-butoxycarbonylaminoethyl)-5-chloro-benzophenone
    2. Synonyms: 2-amino-3'-(2-tert-butoxycarbonylaminoethyl)-5-chloro-benzophenone
    3. CAS NO:214977-59-0
    4. Molecular Formula:
    5. Molecular Weight: 374.867
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 214977-59-0.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: 2-amino-3'-(2-tert-butoxycarbonylaminoethyl)-5-chloro-benzophenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-amino-3'-(2-tert-butoxycarbonylaminoethyl)-5-chloro-benzophenone(214977-59-0)
    11. EPA Substance Registry System: 2-amino-3'-(2-tert-butoxycarbonylaminoethyl)-5-chloro-benzophenone(214977-59-0)
  • 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: 214977-59-0(Hazardous Substances Data)

214977-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214977-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,9,7 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 214977-59:
(8*2)+(7*1)+(6*4)+(5*9)+(4*7)+(3*7)+(2*5)+(1*9)=160
160 % 10 = 0
So 214977-59-0 is a valid CAS Registry Number.

214977-59-0Downstream Products

214977-59-0Relevant articles and documents

4,1-benzoxazepines, their analogues, and their use as somatostatin agonists

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, (2008/06/13)

The present invention provides a compound of the formula: wherein ring A is an optionally substituted aromatic hydrocarbon ring or aromatic heterocyclic ring; ring B is an optionally substituted aromatic hydrocarbon ring or aromatic heterocyclic ring; Z is an optionally substituted cyclic group or linear hydrocarbon group; R1is a hydrogen atom, an optionally substituted hydrocarbon group or heterocyclic ring; R2is an optionally substituted amino group; D is a bond or an optionally substituted divalent hydrocarbon group; E is a bond, —CON(Ra)—, —N(Ra)CO—, —N(Rb)CON(Rc)—, —N(Rd)COO—, —N(Re)SO2—, —COO—, —N(Rf)—, —O—, —S— —SO—, —SO2—, (in which Ra, Rb, Rc, Rd, Reand Rfare respectively a hydrogen atom or an optionally substituted hydrocarbon group); G is a bond or an optionally divalent substituted hydrocarbon group; L is a divalent group; ring B may form an optionally substituted non-aromatic condensed nitrogen-containing heterocyclic ring by combining with R2; X is two hydrogen atoms, an oxygen atom or a sulfur atom;is a single bond or a double bond, and Y is a nitrogen atom whenis a double bond, or an oxygen atom, —N(R4)— (in which R4is a hydrogen atom, an optionally substituted hydrocarbon group or an acyl group) or S(O)n(in which n is 0, 1 or 2) whenis a single bond, or a salt thereof, which have somatostatin receptor agonistic action.

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