184177-77-3

• 

• Basic information

  1. Product Name: Hydrazinecarboxylic acid, (1-ethylpropylidene)-, 1,1-dimethylethyl ester (9CI)
  2. Synonyms: Hydrazinecarboxylic acid, (1-ethylpropylidene)-, 1,1-dimethylethyl ester (9CI);TERT-BUTYL 2-(PENTAN-3-YLIDENE)HYDRAZINECARBOXYLATE
  3. CAS NO:184177-77-3
  4. Molecular Formula: C₁₀H₂₀N₂O₂
  5. Molecular Weight: 200.278
  6. EINECS: N/A
  7. Product Categories: N-BOC
  8. Mol File: 184177-77-3.mol
  9. Article Data: 5

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Hydrazinecarboxylic acid, (1-ethylpropylidene)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Hydrazinecarboxylic acid, (1-ethylpropylidene)-, 1,1-dimethylethyl ester (9CI)(184177-77-3)
  11. EPA Substance Registry System: Hydrazinecarboxylic acid, (1-ethylpropylidene)-, 1,1-dimethylethyl ester (9CI)(184177-77-3)

• 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: 184177-77-3(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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• tert-Butyl 2-(pentan-3-ylidene)hydrazinecarboxylate

  Cas No: 184177-77-3

• No Data

• 10 Milligram

• Amadis Chemical Co., Ltd.
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184177-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184177-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,1,7 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 184177-77:
(8*1)+(7*8)+(6*4)+(5*1)+(4*7)+(3*7)+(2*7)+(1*7)=163
163 % 10 = 3
So 184177-77-3 is a valid CAS Registry Number.

184177-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name	N'-(1-ethylpropylidene)hydrazinecarboxylic acid tert-butyl ester

1.2 Other means of identification

Product number	-
Other names	N'-(1-ethyl-propylidene)-hydrazinecarboxylic acid tert-butyl 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

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:184177-77-3 SDS

184177-77-3Upstream product

• 870-46-2 t-butoxycarbonylhydrazine 
• 96-22-0 pentan-3-one 

184177-77-3Downstream Products

• 184177-78-4 N'-(1-ethylpropyl)hydrazinecarboxylic acid tert-butyl ester 

184177-77-3Relevant articles and documents

A tunable route for the synthesis of azomethine imines and β-aminocarbonyl compounds from alkenes

Clavette, Christian,Gan, Wei,Bongers, Amanda,Markiewicz, Thomas,Toderian, Amy B.,Gorelsky, Serge I.,Beauchemin, Andre M.

supporting information, p. 16111 - 16114,4 (2020/09/09)

Cyclic azomethine imines possessing a β-aminocarbonyl motif are accessed from simple alkene and hydrazone starting materials. A thermal, concerted alkene aminocarbonylation pathway involving an imino-isocyanate intermediate is proposed and supported by DF

FUSED HETEROCYCLIC COMPOUNDS

-

Page/Page column 154, (2008/06/13)

Certain fused pyrrole- and pyrazole-containing heterocyclic compounds are serotonin modulators useful in the treatment of serotonin-mediated diseases.

Novel azapeptide inhibitors of hepatitis C virus serine protease

Bailey, Murray D.,Halmos, Ted,Goudreau, Nathalie,Lescop, Ewen,Llinàs-Brunet, Montse

, p. 3788 - 3799 (2007/10/03)

Azapeptides are known inhibitors of several serine and cysteine proteases. In seeking different classes of inhibitors for the HCV serine protease, a series of novel azapeptide-based inhibitors were investigated which incorporated noncleavable P1/P1′ aza-a

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