Welcome to LookChem.com Sign In|Join Free

CAS

  • or
C28H46N7O19P3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1399774-04-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1399774-04-9 Structure
  • Basic information

    1. Product Name: C28H46N7O19P3S
    2. Synonyms:
    3. CAS NO:1399774-04-9
    4. Molecular Formula:
    5. Molecular Weight: 909.696
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1399774-04-9.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: C28H46N7O19P3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C28H46N7O19P3S(1399774-04-9)
    11. EPA Substance Registry System: C28H46N7O19P3S(1399774-04-9)
  • 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: 1399774-04-9(Hazardous Substances Data)

1399774-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1399774-04-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,9,7,7 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1399774-04:
(9*1)+(8*3)+(7*9)+(6*9)+(5*7)+(4*7)+(3*4)+(2*0)+(1*4)=229
229 % 10 = 9
So 1399774-04-9 is a valid CAS Registry Number.

1399774-04-9Upstream product

1399774-04-9Downstream Products

1399774-04-9Relevant articles and documents

Screening and Engineering the Synthetic Potential of Carboxylating Reductases from Central Metabolism and Polyketide Biosynthesis

Peter, Dominik M.,Schada Von Borzyskowski, Lennart,Kiefer, Patrick,Christen, Philipp,Vorholt, Julia A.,Erb, Tobias J.

, p. 13457 - 13461 (2015)

Carboxylating enoyl-thioester reductases (ECRs) are a recently discovered class of enzymes. They catalyze the highly efficient addition of CO2 to the double bond of α,β-unsaturated CoA-thioesters and serve two biological functions. In primary metabolism of many bacteria they produce ethylmalonyl-CoA during assimilation of the central metabolite acetyl-CoA. In secondary metabolism they provide distinct α-carboxyl-acyl-thioesters to vary the backbone of numerous polyketide natural products. Different ECRs were systematically assessed with a diverse library of potential substrates. We identified three active site residues that distinguish ECRs restricted to C4 and C5-enoyl-CoAs from highly promiscuous ECRs and successfully engineered a selected ECR as proof-of-principle. This study defines the molecular basis of ECR reactivity, allowing for predicting and manipulating a key reaction in natural product diversification.

Post a RFQ

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)

1

What can I do for you?
Get Best Price

Get Best Price for 1399774-04-9