138457-95-1

• 

• Basic information

  1. Product Name: Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)
  2. Synonyms: Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)
  3. CAS NO:138457-95-1
  4. Molecular Formula: C7H13NO2
  5. Molecular Weight: 143.18362
  6. EINECS: N/A
  7. Product Categories: AMINOACID;CARBOXYLICESTER
  8. Mol File: 138457-95-1.mol
  9. Article Data: 3

• 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: Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)(138457-95-1)
  11. EPA Substance Registry System: Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)(138457-95-1)

• 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: 138457-95-1(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

138457-95-1 Suppliers

Recommended suppliersmore

• Product
• FOB Price
• Min.Order
• Supply Ability
• Supplier
• Contact Supplier

138457-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138457-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,5 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138457-95:
(8*1)+(7*3)+(6*8)+(5*4)+(4*5)+(3*7)+(2*9)+(1*5)=161
161 % 10 = 1
So 138457-95-1 is a valid CAS Registry Number.

138457-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	Methyl (1S,2R)-(-)-1-Amino-2-ethyl-1-cyclopropanecarboxylate

1.2 Other means of identification

Product number	-
Other names	(1S,2R)-1-Amino-2-ethyl-cyclopropanecarboxylic acid methyl 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:138457-95-1 SDS

138457-95-1Upstream product

• 138387-14-1 (1SR,3SR,6S)-1-Ethyl-3,6-dihydro-6-isopropyl-5,8-dimethoxy-4,7-diazaspiro<2.5>octane 
• 97935-34-7 Potassium; (1R,2S)-2-ethyl-1-methoxycarbonyl-cyclopropanecarboxylate 
• 87429-74-1 3-Azido-4-ethyl-4,5-dihydro-3H-pyrazole-3-carboxylic acid methyl ester 
• 81852-62-2 Methyl (Z)-2-azido-pentenoate 
• 97935-31-4 2-ethylcyclopropane-1,1-dicarboxylic acid di-tert-butyl ester 
• 18795-92-1 1,1-dimethyl 2-ethylcyclopropane-1,1-dicarboxylate 

138457-95-1Downstream Products

• 63364-55-6 Methyl trans-2-ethyl-1-(N-methoxycarbonylamino)cyclopropanecarboxylate 
• 63364-56-7 (+/-)-(E)-1-amino-2-ethylcyclopropanecarboxylic acid 

138457-95-1Relevant articles and documents

Asymmetric Synthesis via Heterocyclic Intermediates, XLVII. Asymmetric Synthesis of (+)-(1R,2S)-allo-Coronamic Acid

Groth, Ulrich,Halfbrodt, Wolfgang,Schoellkopf, Ulrich

, p. 351 - 356 (2007/10/02)

allo-Coronamic acid (1) was synthesized in five steps enantiomerically and diastereomerically virtually pure by starting from the bislactim ethers of cyclo(-L-Val-Gly-) (3a) or cyclo(-L-tert-Leu-Gly-) (3b) in an overall yield of 31percent.The key step of this synthesis is the intramolecular alkylation of the lithium azaenolate derived from the allylic chloride 4. Key Words: Amino acids / Cyclopropanes / Cyclopropanation, diastereoselective / Bislactim ether method

SYNTHESIS OF 1-AZIDOCYCLOPROPANECARBOXYLATES FROM 2-AZIDO-2-ALKENOATES

Hiyama, Tamejiro,Kai, Mariko

, p. 2103 - 2104 (2007/10/02)

Addition of diazomethane to 2-azido-2-alkenoates followed by pyrolysis of the resulting pyrazoline derivatives affords the title compounds.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
• Urgent purchase

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 138457-95-1 Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)

Send

Send

Metric Ton KG G Pound L ML

Send

Send