14984-42-0

• 

• Basic information

  1. Product Name: 4-amino-3-hydroxyestra-1,3,5(10)-trien-17-one
  2. Synonyms:
  3. CAS NO:14984-42-0
  4. Molecular Formula: C₁₈H₂₃NO₂
  5. Molecular Weight: 285.3807
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 14984-42-0.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 465.9°C at 760 mmHg
  3. Flash Point: 235.6°C
  4. Appearance: N/A
  5. Density: 1.217g/cm³
  6. Vapor Pressure: 2.66E-09mmHg at 25°C
  7. Refractive Index: 1.619
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 4-amino-3-hydroxyestra-1,3,5(10)-trien-17-one(CAS DataBase Reference)
  11. NIST Chemistry Reference: 4-amino-3-hydroxyestra-1,3,5(10)-trien-17-one(14984-42-0)
  12. EPA Substance Registry System: 4-amino-3-hydroxyestra-1,3,5(10)-trien-17-one(14984-42-0)

• 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: 14984-42-0(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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• Estra-1,3,5(10)-trien-17-one,4-amino-3-hydroxy-

  Cas No: 14984-42-0

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• 14984-42-0

  Cas No: 14984-42-0

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• Estra-1,3,5(10)-trien-17-one,4-amino-3-hydroxy- cas 14984-42-0

  Cas No: 14984-42-0

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14984-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14984-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,8 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14984-42:
(7*1)+(6*4)+(5*9)+(4*8)+(3*4)+(2*4)+(1*2)=130
130 % 10 = 0
So 14984-42-0 is a valid CAS Registry Number.

14984-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-amino-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one

1.2 Other means of identification

Product number	-
Other names	4-Aminoestrone

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:14984-42-0 SDS

14984-42-0Upstream product

• 5976-74-9 4-nitroestrone 
• 53-16-7 Estrone 

14984-42-0Downstream Products

• 83873-14-7 (5bS,7aS,10aS,10bR)-2-(4-Bromo-phenylamino)-7a-methyl-5b,6,7,7a,9,10,10a,10b,11,12-decahydro-3-oxa-1-aza-dicyclopenta[a,i]phenathren-8-one 
• 83873-06-7 (5bS,7aS,10aS,10bR)-7a-Methyl-2-p-tolylamino-5b,6,7,7a,9,10,10a,10b,11,12-decahydro-3-oxa-1-aza-dicyclopenta[a,i]phenathren-8-one 
• 83873-02-3 (5bS,7aS,10aS,10bR)-7a-Methyl-2-phenylamino-5b,6,7,7a,9,10,10a,10b,11,12-decahydro-3-oxa-1-aza-dicyclopenta[a,i]phenathren-8-one 
• 83873-12-5 (5bS,7aS,10aS,10bR)-2-(4-Chloro-phenylamino)-7a-methyl-5b,6,7,7a,9,10,10a,10b,11,12-decahydro-3-oxa-1-aza-dicyclopenta[a,i]phenathren-8-one 
• 83873-04-5 (5bS,7aS,10aS,10bR)-7a-Methyl-2-m-tolylamino-5b,6,7,7a,9,10,10a,10b,11,12-decahydro-3-oxa-1-aza-dicyclopenta[a,i]phenathren-8-one 
• 1372799-88-6 C₂₅H₂₇NO₆S₂ 
• 1372799-87-5 4-tosylamidoestrone 
• 40551-34-6 3,4-estrone-o-quinone 
• 83873-00-1 (5bS,7aS,10aS,10bR)-2-Benzylamino-7a-methyl-5b,6,7,7a,9,10,10a,10b,11,12-decahydro-3-oxa-1-aza-dicyclopenta[a,i]phenathren-8-one 
• 83873-08-9 (5bS,7aS,10aS,10bR)-2-(4-Methoxy-phenylamino)-7a-methyl-5b,6,7,7a,9,10,10a,10b,11,12-decahydro-3-oxa-1-aza-dicyclopenta[a,i]phenathren-8-one 

14984-42-0Relevant articles and documents

Synthesis and evaluation of analogues of estrone-3-O-sulfamate as potent steroid sulfatase inhibitors

Lawrence Woo,Leblond, Bertrand,Purohit, Atul,Potter, Barry V.L.

experimental part, p. 2506 - 2519 (2012/06/01)

Estrone sulfamate (EMATE) is a potent irreversible inhibitor of steroid sulfatase (STS). In order to further expand SAR, the compound was substituted at the 2- and/or 4-positions and its 17-carbonyl group was also removed. The following general order of p

Novel 2'-substituted amino-17-oxoestra-1(10),4-dieno[2,3-d]oxazole and estra-1,5(10)-dieno[4,3-d]oxazole derivatives: Synthesis and in vitro anabolic-catabolic activities

Ibrahim El.,Omar

, p. 761 - 768 (2007/10/02)

-

Immunochemical assay method

-

, (2008/06/13)

Haptens and antigen derivatives are coupled, through an azo bond, to proteins to form a conjugated material. The conjugate is injected into laboratory animals to raise antibodies which are useful in immunochemically assaying for the original haptens and a

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